A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611548



Internal ID16398957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452293..74454595hg38UCSC Ensembl
Innerchr8:75364528..75366830hg19UCSC Ensembl
Innerchr8:75527083..75529385hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg382303
hg192303
hg182303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12202n54
Supporting Variantsnssv1116191, nssv1116194, nssv1116192, nssv1116193
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611548
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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