A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568799



Internal ID16009522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326697..31328582hg38UCSC Ensembl
Innerchr15:31618900..31620785hg19UCSC Ensembl
Innerchr15:29406192..29408077hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381886
hg191886
hg181886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839576
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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