A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589775



Internal ID16377184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14545810..14566469hg38UCSC Ensembl
Innerchr3:14587317..14607976hg19UCSC Ensembl
Innerchr3:14562321..14582980hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3820660
hg1920660
hg1820660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151883
SamplesNINDS_66
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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