A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053081



Internal ID19142300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20988783hg38UCSC Ensembl
Innerchr15:20585976..21194112hg19UCSC Ensembl
Innerchr15:18845990..19458771hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38608061
hg19608137
hg18612782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2232n100
Supporting Variantsnssv3537275, nssv3537274
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1053081
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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