A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110056



Internal ID15963242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375062..39507199hg38UCSC Ensembl
Innerchr8:39232581..39364718hg19UCSC Ensembl
Innerchr8:39351738..39483875hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38132138
hg19132138
hg18132138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610968
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110056
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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