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nsv5491852

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:332,087

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2507 SVs from 110 studies. See in: genome view    
Submitted genomic6,543,199-6,875,285Question Mark
Overlapping variant regions from other studies: 2511 SVs from 110 studies. See in: genome view    
Remapped(Score: Perfect):6,543,199-6,875,285Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491852Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr96,543,1996,875,285
nsv5491852RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr96,543,1996,875,285

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019669duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019669Submitted genomicNC_000009.12:g.654
3199_6875285dup
GRCh38 (hg38)NC_000009.12Chr96,543,1996,875,285
nssv17019669RemappedPerfectNC_000009.11:g.654
3199_6875285dup
GRCh37.p13First PassNC_000009.11Chr96,543,1996,875,285

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)
nssv17019669<0.00126404
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