A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671338



Internal ID15061304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:35313591..35621950hg38UCSC Ensembl
Innerchr8:35171109..35479468hg19UCSC Ensembl
Innerchr8:35290651..35599010hg18UCSC Ensembl
Innerchr8:35290651..35599010hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38308360
hg19308360
hg18308360
hg17308360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520421
Supporting Variants
Samples
Known GenesUNC5D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671338
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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