A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601272



Internal ID16041995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29886431..29893503hg38UCSC Ensembl
Innerchr6:29854208..29861280hg19UCSC Ensembl
Innerchr6:29962187..29969259hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg387073
hg197073
hg187073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051813
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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