A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579339



Internal ID16366748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33780600..33818627hg38UCSC Ensembl
Innerchr19:34271505..34309532hg19UCSC Ensembl
Innerchr19:38963345..39001372hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3838028
hg1938028
hg1838028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898557
Samples
Known GenesKCTD15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579339
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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