A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697201



Internal ID15087167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45566781..45570959hg38UCSC Ensembl
Innerchr19:46070039..46074217hg19UCSC Ensembl
Innerchr19:50761879..50766057hg18UCSC Ensembl
Innerchr19:50761879..50766057hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384179
hg194179
hg184179
hg174179
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520061
Supporting Variants
Samples
Known GenesOPA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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