A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052164



Internal ID19141383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..20806746hg38UCSC Ensembl
Innerchr15:20291301..21012075hg19UCSC Ensembl
Innerchr15:18551315..19272115hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38720699
hg19720775
hg18720801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2195n100
Supporting Variantsnssv3537918
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052164
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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