A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604015



Internal ID16391424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78810125..78816254hg38UCSC Ensembl
Innerchr6:79519842..79525971hg19UCSC Ensembl
Innerchr6:79576561..79582690hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386130
hg196130
hg186130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10820n54
Supporting Variantsnssv1066957, nssv1066959, nssv1066958
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604015
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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