A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117020



Internal ID15623520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78807362..79006224hg38UCSC Ensembl
Innerchr8:79719597..79918459hg19UCSC Ensembl
Innerchr8:79882152..80081014hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38198863
hg19198863
hg18198863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611578
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)nssv1117020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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