A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837126



Internal ID16131082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20344556..20890798hg38UCSC Ensembl
Innerchr15:20549809..21096127hg19UCSC Ensembl
Innerchr15:18809823..19360786hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38546243
hg19546319
hg18550964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567329
Supporting Variants
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837126
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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