A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601228



Internal ID16041951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29528443..29532510hg38UCSC Ensembl
Innerchr6:29496220..29500287hg19UCSC Ensembl
Innerchr6:29604199..29608266hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384068
hg194068
hg184068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051674
Samples
Known GenesLINC01015
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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