A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568773



Internal ID16009496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31324471..31327665hg38UCSC Ensembl
Innerchr15:31616674..31619868hg19UCSC Ensembl
Innerchr15:29403966..29407160hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383195
hg193195
hg183195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839501
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568773
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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