A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117008



Internal ID15970194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77475007..77539986hg38UCSC Ensembl
Innerchr8:78387243..78452222hg19UCSC Ensembl
Innerchr8:78549798..78614777hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3864980
hg1964980
hg1864980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611567
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1117008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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