A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568789



Internal ID16009512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326081..31328232hg38UCSC Ensembl
Innerchr15:31618284..31620435hg19UCSC Ensembl
Innerchr15:29405576..29407727hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382152
hg192152
hg182152
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4431n54
Supporting Variantsnssv839558, nssv839562, nssv839557, nssv839561, nssv839556, nssv839560, nssv839559
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568789
Frequency
Sample Size17421
Observed Gain2
Observed Loss5
Observed Complex0
Frequencyn/a


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