A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568774



Internal ID16009497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31324471..31328740hg38UCSC Ensembl
Innerchr15:31616674..31620943hg19UCSC Ensembl
Innerchr15:29403966..29408235hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg384270
hg194270
hg184270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839502
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568774
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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