A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610732



Internal ID16051455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996177..18999930hg38UCSC Ensembl
Innerchr8:18853687..18857440hg19UCSC Ensembl
Innerchr8:18897967..18901720hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg383754
hg193754
hg183754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12050n54
Supporting Variantsnssv1107447
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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