A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569402



Internal ID16356811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50726920..50825327hg38UCSC Ensembl
Innerchr15:51019117..51117524hg19UCSC Ensembl
Innerchr15:48806409..48904816hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3898408
hg1998408
hg1898408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148864
SamplesHGDP00977
Known GenesSPPL2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569402
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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