A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156619



Internal ID15879552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82399997..82492913hg38UCSC Ensembl
Innerchr8:83312232..83405148hg19UCSC Ensembl
Innerchr8:83474787..83567703hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3892917
hg1992917
hg1892917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611619
Supporting Variants
SamplesHGDP01385
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156619
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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