A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148866



Internal ID15533806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51562521..51684962hg38UCSC Ensembl
Innerchr15:51854718..51977159hg19UCSC Ensembl
Innerchr15:49642010..49764451hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38122442
hg19122442
hg18122442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569407
Supporting Variants
SamplesNINDS_219
Known GenesDMXL2, SCG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148866
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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