A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519462



Internal ID15446755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:23844534..23851677hg38UCSC Ensembl
Innerchr6:23844762..23851905hg19UCSC Ensembl
Innerchr6:23952741..23959884hg18UCSC Ensembl
Innerchr6:23952741..23959884hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg387144
hg197144
hg187144
hg177144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694330
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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