A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568792



Internal ID16009515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326081..31328740hg38UCSC Ensembl
Innerchr15:31618284..31620943hg19UCSC Ensembl
Innerchr15:29405576..29408235hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382660
hg192660
hg182660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n54
Supporting Variantsnssv839565, nssv839567, nssv839566
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568792
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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