A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045512



Internal ID19134731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20441310..20828285hg38UCSC Ensembl
Innerchr15:20646563..21033614hg19UCSC Ensembl
Innerchr15:18906577..19296118hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38386976
hg19387052
hg18389542
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2257n100
Supporting Variantsnssv3540866
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045512
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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