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nsv1161886

  • Variant Calls:25
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,465

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 687 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):169,247,699-169,273,163Question Mark
Overlapping variant regions from other studies: 690 SVs from 73 studies. See in: genome view    
Submitted genomic169,216,937-169,242,401Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv1161886RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nsv1161886Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv4030043deletionSNP arrayProbe signal intensity1
nssv4030044deletionSNP arrayProbe signal intensity1
nssv4030045deletionSNP arrayProbe signal intensity1
nssv4030046deletionSNP arrayProbe signal intensity1
nssv4030047deletionSNP arrayProbe signal intensity1
nssv4030049deletionSNP arrayProbe signal intensity1
nssv4030050deletionSNP arrayProbe signal intensity0
nssv4030051deletionSNP arrayProbe signal intensity1
nssv4030052deletionSNP arrayProbe signal intensity1
nssv4030053deletionSNP arrayProbe signal intensity1
nssv4030054deletionSNP arrayProbe signal intensity1
nssv4030055deletionSNP arrayProbe signal intensity1
nssv4030056deletionSNP arrayProbe signal intensity1
nssv4030057deletionSNP arrayProbe signal intensity1
nssv4030058deletionSNP arrayProbe signal intensity1
nssv4030060deletionSNP arrayProbe signal intensity1
nssv4030061deletionSNP arrayProbe signal intensity1
nssv4030062deletionSNP arrayProbe signal intensity1
nssv4030063deletionSNP arrayProbe signal intensity1
nssv4030064duplicationSNP arrayProbe signal intensity3
nssv4030065deletionSNP arrayProbe signal intensity1
nssv4030066deletionSNP arrayProbe signal intensity1
nssv4030067deletionSNP arrayProbe signal intensity1
nssv4030068deletionSNP arrayProbe signal intensity1
nssv4030069deletionSNP arrayProbe signal intensity1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv4030043RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030044RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030045RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030046RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030047RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030049RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030050RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030051RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030052RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030053RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030054RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030055RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030056RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030057RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030058RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030060RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030061RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030062RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030063RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030064RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)dup
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030065RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030066RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030067RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030068RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030069RemappedPerfectNC_000001.11:g.(16
9247699_169264736)
_(169272528_169273
163)del
GRCh38.p12First PassNC_000001.11Chr1169,247,699169,264,736169,272,528169,273,163
nssv4030043Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030044Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030045Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030046Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030047Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030049Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030050Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030051Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030052Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030053Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030054Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030055Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030056Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030057Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030058Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030060Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030061Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030062Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030063Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030064Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)dup
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030065Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030066Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030067Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030068Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401
nssv4030069Submitted genomicNC_000001.10:g.(16
9216937_169233974)
_(169241766_169242
401)del
GRCh37 (hg19)NC_000001.10Chr1169,216,937169,233,974169,241,766169,242,401

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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