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nsv5901763

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 37 studies. See in: genome view    
Submitted genomic27,547,704-27,547,773Question Mark
Overlapping variant regions from other studies: 132 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):27,515,483-27,515,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5901763Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr627,547,70427,547,773
nsv5901763RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr627,515,48327,515,552

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17438208duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17438208Submitted genomicNC_000006.12:g.275
47704_27547773dup
GRCh38 (hg38)NC_000006.12Chr627,547,70427,547,773
nssv17438208RemappedPerfectNC_000006.11:g.275
15483_27515552dup
GRCh37.p13First PassNC_000006.11Chr627,515,48327,515,552

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)
nssv174382080.00121652
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