A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107456



Internal ID15613956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996430..19011922hg38UCSC Ensembl
Innerchr8:18853940..18869432hg19UCSC Ensembl
Innerchr8:18898220..18913712hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815493
hg1915493
hg1815493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610742
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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