A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv836889



Internal ID16130845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20010432..21065301hg38UCSC Ensembl
Innerchr15:20215685..21270630hg19UCSC Ensembl
Innerchr15:18475699..19535289hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381054870
hg191054946
hg181059591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567154
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv836889
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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