A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110059



Internal ID15963245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375062..39520881hg38UCSC Ensembl
Innerchr8:39232581..39378400hg19UCSC Ensembl
Innerchr8:39351738..39497557hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38145820
hg19145820
hg18145820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610970
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)nssv1110059
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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