A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698293



Internal ID15088259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74590778..74670785hg38UCSC Ensembl
Innerchr10:76350536..76430543hg19UCSC Ensembl
Innerchr10:76020542..76100549hg18UCSC Ensembl
Innerchr10:76020542..76100549hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3880008
hg1980008
hg1880008
hg1780008
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515824
Supporting Variants
Samples
Known GenesADK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698293
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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