A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612379



Internal ID16399788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136670241..136844029hg38UCSC Ensembl
Innerchr8:137682484..137856272hg19UCSC Ensembl
Innerchr8:137751666..137925454hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38173789
hg19173789
hg18173789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122223, nssv1122219, nssv1122220, nssv1122221, nssv1122222, nssv1122227, nssv1122226, nssv1122228, nssv1122230, nssv1122229, nssv1122224, nssv1122225
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612379
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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