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nsv511663

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,174

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 610 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):155,687,184-155,709,357Question Mark
Overlapping variant regions from other studies: 599 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):154,916,845-154,939,018Question Mark
Overlapping variant regions from other studies: 273 SVs from 14 studies. See in: genome view    
Submitted genomic154,570,039-154,592,212Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv511663RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX155,687,184155,688,696155,691,896155,709,357
nsv511663RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX154,916,845154,918,357154,921,557154,939,018
nsv511663Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000023.9ChrX154,570,039154,571,551154,574,751154,592,212

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv626300copy number gain1SNP arraySNP genotyping analysis2,637

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv626300RemappedPerfectNC_000023.11:g.(15
5687184_155688696)
_(155691896_155709
357)dup
GRCh38.p12First PassNC_000023.11ChrX155,687,184155,688,696155,691,896155,709,357
nssv626300RemappedPerfectNC_000023.10:g.(15
4916845_154918357)
_(154921557_154939
018)dup
GRCh37.p13First PassNC_000023.10ChrX154,916,845154,918,357154,921,557154,939,018
nssv626300Submitted genomicNC_000023.9:g.(154
570039_154571551)_
(154574751_1545922
12)dup
NCBI36 (hg18)NC_000023.9ChrX154,570,039154,571,551154,574,751154,592,212

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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