A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604016



Internal ID16391425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78810125..78816552hg38UCSC Ensembl
Innerchr6:79519842..79526269hg19UCSC Ensembl
Innerchr6:79576561..79582988hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386428
hg196428
hg186428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10820n54
Supporting Variantsnssv1066960, nssv1066962, nssv1066961, nssv1066963
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604016
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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