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nsv5504091

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,956

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 192 SVs from 46 studies. See in: genome view    
Submitted genomic9,603,579-9,613,534Question Mark
Overlapping variant regions from other studies: 192 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):9,756,175-9,766,130Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504091Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,603,5799,613,534
nsv5504091RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr129,756,1759,766,130

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052827deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052827Submitted genomicNC_000012.12:g.960
3579_9613534del
GRCh38 (hg38)NC_000012.12Chr129,603,5799,613,534
nssv17052827RemappedPerfectNC_000012.11:g.975
6175_9766130del
GRCh37.p13First PassNC_000012.11Chr129,756,1759,766,130

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17052827<0.00136404
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