U.S. flag

An official website of the United States government

nsv6287754

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 75 SVs from 23 studies. See in: genome view    
Submitted genomic95,529,315-95,529,315Question Mark
Overlapping variant regions from other studies: 75 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):95,923,091-95,923,091Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6287754Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1295,529,31595,529,315
nsv6287754RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1295,923,09195,923,091

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17928668insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17928668Submitted genomicNC_000012.12:g.955
29315_95529316ins5
6
GRCh38 (hg38)NC_000012.12Chr1295,529,31595,529,315
nssv17928668RemappedPerfectNC_000012.11:g.959
23091_95923092ins5
6
GRCh37.p13First PassNC_000012.11Chr1295,923,09195,923,091

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)
nssv17928668<0.00112340
Support Center