A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156139



Internal ID15531109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98049764..98103973hg38UCSC Ensembl
Innerchr8:99061992..99116201hg19UCSC Ensembl
Innerchr8:99131168..99185377hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3854210
hg1954210
hg1854210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611805
Supporting Variants
SamplesHGDP01047
Known GenesC8orf47, HRSP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156139
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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