A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149556



Internal ID15533206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31329118..31405439hg38UCSC Ensembl
Innerchr15:31621321..31697642hg19UCSC Ensembl
Innerchr15:29408613..29484934hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3876322
hg1976322
hg1876322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568801
Supporting Variants
SamplesNINDS_124
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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