A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601502



Internal ID16388911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269452..31330966hg38UCSC Ensembl
Innerchr6:31237229..31298743hg19UCSC Ensembl
Innerchr6:31345208..31406722hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3861515
hg1961515
hg1861515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1052305
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601502
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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