A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704126



Internal ID15094092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133969020..133977441hg38UCSC Ensembl
Innerchr3:133687864..133696285hg19UCSC Ensembl
Innerchr3:135170554..135178975hg18UCSC Ensembl
Innerchr3:135170562..135178983hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg388422
hg198422
hg188422
hg178422
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527655
Supporting Variants
Samples
Known GenesSLCO2A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704126
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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