A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610931



Internal ID16398340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:34318956..34368697hg38UCSC Ensembl
Innerchr8:34176474..34226215hg19UCSC Ensembl
Innerchr8:34296016..34345757hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3849742
hg1949742
hg1849742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109988
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610931
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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