A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610729



Internal ID16051452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994964..19000632hg38UCSC Ensembl
Innerchr8:18852474..18858142hg19UCSC Ensembl
Innerchr8:18896754..18902422hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385669
hg195669
hg185669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12047n54
Supporting Variantsnssv1107436
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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