A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521886



Internal ID15449179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13704939..13721779hg38UCSC Ensembl
Innerchr7:13744564..13761404hg19UCSC Ensembl
Innerchr7:13711089..13727929hg18UCSC Ensembl
Innerchr7:13517804..13534644hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3816841
hg1916841
hg1816841
hg1716841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv408n21
Supporting Variantsnssv694657
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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