A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601230



Internal ID16388639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29721813..29732406hg38UCSC Ensembl
Innerchr6:29689590..29700183hg19UCSC Ensembl
Innerchr6:29797569..29808162hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3810594
hg1910594
hg1810594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154038
SamplesHGDP00891
Known GenesHLA-F, HLA-F-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601230
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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