A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051642



Internal ID19140861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20988783hg38UCSC Ensembl
Innerchr15:20216943..21194112hg19UCSC Ensembl
Innerchr15:18476957..19458771hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38977094
hg19977170
hg18981815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2188n100
Supporting Variantsnssv3536977
Samples
Known GenesCHEK2P2, CT60, 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)nsv1051642
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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