A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601930



Internal ID16042653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31415294..31462366hg38UCSC Ensembl
Innerchr6:31383071..31430143hg19UCSC Ensembl
Innerchr6:31491050..31538122hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3847073
hg1947073
hg1847073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10459n54
Supporting Variantsnssv1053512
Samples
Known GenesMICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601930
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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