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nsv6141806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 214 SVs from 53 studies. See in: genome view    
Submitted genomic128,052,552-128,060,552Question Mark
Overlapping variant regions from other studies: 214 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):130,814,831-130,822,831Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6141806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9128,052,552128,060,552
nsv6141806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9130,814,831130,822,831

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027272duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027272Submitted genomicNC_000009.12:g.128
052552_128060552du
p
GRCh38 (hg38)NC_000009.12Chr9128,052,552128,060,552
nssv17027272RemappedPerfectNC_000009.11:g.130
814831_130822831du
p
GRCh37.p13First PassNC_000009.11Chr9130,814,831130,822,831

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)
nssv17027272<0.00146338
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