A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963373



Internal ID15910643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58491538..58492211hg38UCSC Ensembl
Innerchr3:58477265..58477938hg19UCSC Ensembl
Innerchr3:58452305..58452978hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38674
hg19674
hg18674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590374
Supporting Variants
Samples
Known GenesKCTD6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963373
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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