A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041020



Internal ID19130239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20190264..20886842hg38UCSC Ensembl
Innerchr15:20395517..21092171hg19UCSC Ensembl
Innerchr15:18655531..19356830hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38696579
hg19696655
hg18701300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2211n100
Supporting Variantsnssv3716439
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041020
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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