A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601891



Internal ID16042614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392478..31489856hg38UCSC Ensembl
Innerchr6:31360255..31457633hg19UCSC Ensembl
Innerchr6:31468234..31565612hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3897379
hg1997379
hg1897379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10454n54
Supporting Variantsnssv1053418
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601891
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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