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nsv6214652

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:162

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 25 studies. See in: genome view    
Submitted genomic17,103,690-17,103,851Question Mark
Overlapping variant regions from other studies: 162 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):17,584,580-17,584,741Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6214652Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2217,103,69017,103,851
nsv6214652RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2217,584,58017,584,741

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17946702deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17946702Submitted genomicNC_000022.11:g.171
03690_17103851del
GRCh38 (hg38)NC_000022.11Chr2217,103,69017,103,851
nssv17946702RemappedPerfectNC_000022.10:g.175
84580_17584741del
GRCh37.p13First PassNC_000022.10Chr2217,584,58017,584,741

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)
nssv17946702<0.00122254
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