A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610961



Internal ID16398370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374115..39520881hg38UCSC Ensembl
Innerchr8:39231634..39378400hg19UCSC Ensembl
Innerchr8:39350791..39497557hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38146767
hg19146767
hg18146767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12093n54
Supporting Variantsnssv1110035, nssv1110034
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610961
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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