A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610797



Internal ID16398206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25115293..25129006hg38UCSC Ensembl
Innerchr8:24972808..24986521hg19UCSC Ensembl
Innerchr8:25028725..25042438hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3813714
hg1913714
hg1813714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12062n54
Supporting Variantsnssv1107525, nssv1107524
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610797
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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