A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610731



Internal ID16051454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994964..19006355hg38UCSC Ensembl
Innerchr8:18852474..18863865hg19UCSC Ensembl
Innerchr8:18896754..18908145hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3811392
hg1911392
hg1811392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12049n54
Supporting Variantsnssv1107438, nssv1107442, nssv1107446, nssv1107445, nssv1107440, nssv1107441, nssv1107444, nssv1107439, nssv1107443
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610731
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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