A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106774



Internal ID15959960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13178896..13225236hg38UCSC Ensembl
Innerchr8:13036405..13082745hg19UCSC Ensembl
Innerchr8:13080776..13127116hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3846341
hg1946341
hg1846341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610413
Supporting Variants
Samples
Known GenesDLC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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