A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110049



Internal ID15963235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375062..39386523hg38UCSC Ensembl
Innerchr8:39232581..39244042hg19UCSC Ensembl
Innerchr8:39351738..39363199hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3811462
hg1911462
hg1811462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610964
Supporting Variants
Samples
Known GenesADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110049
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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