A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568781



Internal ID16009504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325674..31328740hg38UCSC Ensembl
Innerchr15:31617877..31620943hg19UCSC Ensembl
Innerchr15:29405169..29408235hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383067
hg193067
hg183067
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839535, nssv839530, nssv839528, nssv839529, nssv839533, nssv839534, nssv839532, nssv839531
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568781
Frequency
Sample Size17421
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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