A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589758



Internal ID16377167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13639712..13675753hg38UCSC Ensembl
Innerchr3:13681212..13717252hg19UCSC Ensembl
Innerchr3:13656213..13692253hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3836042
hg1936041
hg1836041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959419
Samples
Known GenesLINC00620
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589758
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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