A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568777



Internal ID16009500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325674..31327742hg38UCSC Ensembl
Innerchr15:31617877..31619945hg19UCSC Ensembl
Innerchr15:29405169..29407237hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382069
hg192069
hg182069
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839507, nssv839506, nssv839508, nssv839509, nssv839510
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568777
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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