U.S. flag

An official website of the United States government

nsv6261568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:275

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 24 studies. See in: genome view    
Submitted genomic177,945,702-177,945,976Question Mark
Overlapping variant regions from other studies: 153 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):178,810,429-178,810,703Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6261568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2177,945,702177,945,976
nsv6261568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2178,810,429178,810,703

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17878468deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17878468Submitted genomicNC_000002.12:g.177
945702_177945976de
l
GRCh38 (hg38)NC_000002.12Chr2177,945,702177,945,976
nssv17878468RemappedPerfectNC_000002.11:g.178
810429_178810703de
l
GRCh37.p13First PassNC_000002.11Chr2178,810,429178,810,703

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)
nssv17878468<0.00122310
Support Center