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nsv6215915

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:284

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 307 SVs from 28 studies. See in: genome view    
Submitted genomic49,781,915-49,782,198Question Mark
Overlapping variant regions from other studies: 307 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):50,175,563-50,175,846Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6215915Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2249,781,91549,782,198
nsv6215915RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2250,175,56350,175,846

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17953109deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17953109Submitted genomicNC_000022.11:g.497
81915_49782198del
GRCh38 (hg38)NC_000022.11Chr2249,781,91549,782,198
nssv17953109RemappedPerfectNC_000022.10:g.501
75563_50175846del
GRCh37.p13First PassNC_000022.10Chr2250,175,56350,175,846

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)
nssv17953109<0.00112222
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