A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837104



Internal ID16131060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20242941..22161108hg38UCSC Ensembl
Innerchr15:20448194..22449059hg19UCSC Ensembl
Innerchr15:18708208..19950423hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381918168
hg192000866
hg181242216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567311
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837104
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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