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nsv2803233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,094

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 605 SVs from 78 studies. See in: genome view    
Submitted genomic22,282,581-22,293,674Question Mark
Overlapping variant regions from other studies: 603 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):23,654,901-23,665,994Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2803233Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2122,282,58122,293,674
nsv2803233RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2123,654,90123,665,994

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13702124deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13702124Submitted genomicNC_000021.9:g.2228
2581_22293674del11
094
GRCh38 (hg38)NC_000021.9Chr2122,282,58122,293,674
nssv13702124RemappedPerfectNC_000021.8:g.2365
4901_23665994del11
094
GRCh37.p13First PassNC_000021.8Chr2123,654,90123,665,994

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)
nssv137021240.1561064
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