A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117009



Internal ID15970195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77539986..77639466hg38UCSC Ensembl
Innerchr8:78452222..78551702hg19UCSC Ensembl
Innerchr8:78614777..78714257hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3899481
hg1999481
hg1899481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611568
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)nssv1117009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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