A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1112242



Internal ID15618742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:41793950..41827648hg38UCSC Ensembl
Innerchr8:41651468..41685166hg19UCSC Ensembl
Innerchr8:41770625..41804323hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3833699
hg1933699
hg1833699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611130
Supporting Variants
Samples
Known GenesANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1112242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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