A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610735



Internal ID16051458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996177..19000683hg38UCSC Ensembl
Innerchr8:18853687..18858193hg19UCSC Ensembl
Innerchr8:18897967..18902473hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg384507
hg194507
hg184507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12050n54
Supporting Variantsnssv1107450
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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