A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610720



Internal ID16051443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18895083..19132225hg38UCSC Ensembl
Innerchr8:18752593..18989735hg19UCSC Ensembl
Innerchr8:18796873..19034015hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38237143
hg19237143
hg18237143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156348
SamplesHGDP01405
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610720
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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