A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044144



Internal ID19133363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20190264..20844186hg38UCSC Ensembl
Innerchr15:20395517..21049515hg19UCSC Ensembl
Innerchr15:18655531..19314115hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38653923
hg19653999
hg18658585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2210n100
Supporting Variantsnssv3538030
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)nsv1044144
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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