A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106773



Internal ID15613273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13121891..13662651hg38UCSC Ensembl
Innerchr8:12979400..13520160hg19UCSC Ensembl
Innerchr8:13023771..13564531hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38540761
hg19540761
hg18540761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610412
Supporting Variants
Samples
Known GenesC8orf48, DLC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106773
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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