A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590376



Internal ID16377785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58491707..58492513hg38UCSC Ensembl
Innerchr3:58477434..58478240hg19UCSC Ensembl
Innerchr3:58452474..58453280hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38807
hg19807
hg18807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963375
Samples
Known GenesKCTD6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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