A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601456



Internal ID16388865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29941782..29950322hg38UCSC Ensembl
Innerchr6:29909559..29918099hg19UCSC Ensembl
Innerchr6:30017538..30026078hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg388541
hg198541
hg188541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10364n54
Supporting Variantsnssv1052232
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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