A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601224



Internal ID16388633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29376927..29388810hg38UCSC Ensembl
Innerchr6:29344704..29356587hg19UCSC Ensembl
Innerchr6:29452683..29464566hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3811884
hg1911884
hg1811884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051670
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601224
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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