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nsv1161837

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93,779

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2329 SVs from 91 studies. See in: genome view    
Remapped(Score: Perfect):12,007,658-12,101,436Question Mark
Overlapping variant regions from other studies: 2333 SVs from 91 studies. See in: genome view    
Submitted genomic12,007,658-12,101,436Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv1161837RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr912,007,65812,008,57712,099,45812,101,436
nsv1161837Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr912,007,65812,008,57712,099,45812,101,436

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv4037352deletionSNP arrayProbe signal intensity1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv4037352RemappedPerfectNC_000009.12:g.(12
007658_12008577)_(
12099458_12101436)
del
GRCh38.p12First PassNC_000009.12Chr912,007,65812,008,57712,099,45812,101,436
nssv4037352Submitted genomicNC_000009.11:g.(12
007658_12008577)_(
12099458_12101436)
del
GRCh37 (hg19)NC_000009.11Chr912,007,65812,008,57712,099,45812,101,436

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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