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nsv2805841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,211

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 554 SVs from 64 studies. See in: genome view    
Submitted genomic179,200,725-179,216,935Question Mark
Overlapping variant regions from other studies: 554 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):180,065,452-180,081,662Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2805841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2179,200,725179,216,935
nsv2805841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2180,065,452180,081,662

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13677705deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13677705Submitted genomicNC_000002.12:g.179
200725_179216935de
l16211
GRCh38 (hg38)NC_000002.12Chr2179,200,725179,216,935
nssv13677705RemappedPerfectNC_000002.11:g.180
065452_180081662de
l16211
GRCh37.p13First PassNC_000002.11Chr2180,065,452180,081,662

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)
nssv136777050.3752464
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