A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682326



Internal ID15072292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55354159..55376298hg38UCSC Ensembl
Innerchr19:55865527..55887666hg19UCSC Ensembl
Innerchr19:60557339..60579478hg18UCSC Ensembl
Innerchr19:60557339..60579478hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3822140
hg1922140
hg1822140
hg1722140
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516199
Supporting Variants
Samples
Known GenesCOX6B2, FAM71E2, IL11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682326
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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