A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589967



Internal ID16377376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26004870..26182680hg38UCSC Ensembl
Innerchr3:26046361..26224171hg19UCSC Ensembl
Innerchr3:26021365..26199175hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38177811
hg19177811
hg18177811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960143
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589967
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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