A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610726



Internal ID16051449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994964..19000155hg38UCSC Ensembl
Innerchr8:18852474..18857665hg19UCSC Ensembl
Innerchr8:18896754..18901945hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385192
hg195192
hg185192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12047n54
Supporting Variantsnssv1107432, nssv1107433
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610726
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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