A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589856



Internal ID16377265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20263740..20395001hg38UCSC Ensembl
Innerchr3:20305232..20436493hg19UCSC Ensembl
Innerchr3:20280236..20411497hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38131262
hg19131262
hg18131262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151744
SamplesNINDS_216
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589856
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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