A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039193



Internal ID19128412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20936927hg38UCSC Ensembl
Innerchr15:20284054..21142256hg19UCSC Ensembl
Innerchr15:18544068..19406915hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38858127
hg19858203
hg18862848
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2189n100
Supporting Variantsnssv3536555, nssv3715984
Samples
Known GenesCHEK2P2, 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)nsv1039193
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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