A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610783



Internal ID16398192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:24247754..24280615hg38UCSC Ensembl
Innerchr8:24105267..24138128hg19UCSC Ensembl
Innerchr8:24161212..24194073hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3832862
hg1932862
hg1832862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12058n54
Supporting Variantsnssv1107485
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610783
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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