A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963377



Internal ID16257333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58491763..58492513hg38UCSC Ensembl
Innerchr3:58477490..58478240hg19UCSC Ensembl
Innerchr3:58452530..58453280hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38751
hg19751
hg18751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590377
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)nssv963377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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