nsv5473551

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
Submitted genomic159,796,295-159,796,370Question Mark
Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):160,217,327-160,217,402Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473551Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6159,796,295159,796,370
nsv5473551RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,217,327160,217,402

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16989213deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16989213Submitted genomicNC_000006.12:g.159
796295_159796370de
l
GRCh38 (hg38)NC_000006.12Chr6159,796,295159,796,370
nssv16989213RemappedPerfectNC_000006.11:g.160
217327_160217402de
l
GRCh37.p13First PassNC_000006.11Chr6160,217,327160,217,402

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)
nssv16989213<0.00156404
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