A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611638



Internal ID16399047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83307039..83375018hg38UCSC Ensembl
Innerchr8:84219274..84287253hg19UCSC Ensembl
Innerchr8:84381829..84449808hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3867980
hg1967980
hg1867980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12219n54
Supporting Variantsnssv1117331, nssv1117332, nssv1117333
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611638
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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