A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837255



Internal ID16131211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380145..20689298hg38UCSC Ensembl
Innerchr15:20585398..20894627hg19UCSC Ensembl
Innerchr15:18845412..19191595hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38309154
hg19309230
hg18346184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567428
Supporting Variants
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837255
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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