A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568775



Internal ID16009498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325585..31327441hg38UCSC Ensembl
Innerchr15:31617788..31619644hg19UCSC Ensembl
Innerchr15:29405080..29406936hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381857
hg191857
hg181857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4429n54
Supporting Variantsnssv839503
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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