A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156858



Internal ID15875097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:70986138..71051176hg38UCSC Ensembl
Innerchr8:71898373..71963411hg19UCSC Ensembl
Innerchr8:72060927..72125965hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3865039
hg1965039
hg1865039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611489
Supporting Variants
SamplesHGDP00635
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156858
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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