A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051676



Internal ID19140895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20190264..20996195hg38UCSC Ensembl
Innerchr15:20395517..21201524hg19UCSC Ensembl
Innerchr15:18655531..19466183hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38805932
hg19806008
hg18810653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2212n100
Supporting Variantsnssv3538039, nssv3538038, nssv3538037
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)nsv1051676
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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