A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601684



Internal ID16389093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31315520..31354129hg38UCSC Ensembl
Innerchr6:31283297..31321906hg19UCSC Ensembl
Innerchr6:31391276..31429885hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3838610
hg1938610
hg1838610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053053, nssv1053052
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601684
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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