A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689964



Internal ID15426616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78769445..78778752hg38UCSC Ensembl
Innerchr10:80529202..80538509hg19UCSC Ensembl
Innerchr10:80199208..80208515hg18UCSC Ensembl
Innerchr10:80199208..80208515hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg389308
hg199308
hg189308
hg179308
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517525
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689964
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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