A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601288



Internal ID16042011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29888161..29928882hg38UCSC Ensembl
Innerchr6:29855938..29896659hg19UCSC Ensembl
Innerchr6:29963917..30004638hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3840722
hg1940722
hg1840722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10348n54
Supporting Variantsnssv1051834
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601288
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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