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nsv6207224

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 216 SVs from 41 studies. See in: genome view    
Submitted genomic75,558,859-75,558,925Question Mark
Overlapping variant regions from other studies: 216 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):73,554,940-73,555,006Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6207224Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,558,85975,558,925
nsv6207224RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,554,94073,555,006

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17934312deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17934312Submitted genomicNC_000017.11:g.755
58859_75558925del
GRCh38 (hg38)NC_000017.11Chr1775,558,85975,558,925
nssv17934312RemappedPerfectNC_000017.10:g.735
54940_73555006del
GRCh37.p13First PassNC_000017.10Chr1773,554,94073,555,006

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)
nssv179343120.00121684
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