A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610725



Internal ID16051448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994964..19000098hg38UCSC Ensembl
Innerchr8:18852474..18857608hg19UCSC Ensembl
Innerchr8:18896754..18901888hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385135
hg195135
hg185135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12047n54
Supporting Variantsnssv1107431, nssv1107425, nssv1107429, nssv1107430, nssv1107424, nssv1107427, nssv1107428, nssv1107426
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610725
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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