A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568772



Internal ID16009495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31245293..31345793hg38UCSC Ensembl
Innerchr15:31537496..31637996hg19UCSC Ensembl
Innerchr15:29324788..29425288hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38100501
hg19100501
hg18100501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149555
Samples1780862540_A
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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