A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105862



Internal ID15612362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7860665..8183644hg38UCSC Ensembl
Innerchr8:7718187..8041166hg19UCSC Ensembl
Innerchr8:7755597..8078576hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38322980
hg19322980
hg18322980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610137
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB109P1B, DEFB4A, FAM66E, MIR548I3, SPAG11A, USP17L3, USP17L8, ZNF705B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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