A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589841



Internal ID16030564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17172578..17248973hg38UCSC Ensembl
Innerchr3:17214070..17290465hg19UCSC Ensembl
Innerchr3:17189074..17265469hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3876396
hg1976396
hg1876396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959848
Samples
Known GenesTBC1D5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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