A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610721



Internal ID16051444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18981254..19094312hg38UCSC Ensembl
Innerchr8:18838764..18951822hg19UCSC Ensembl
Innerchr8:18883044..18996102hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38113059
hg19113059
hg18113059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107415
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610721
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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