A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537266



Internal ID18835547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20929146hg38UCSC Ensembl
Innerchr15:20585976..21134475hg19UCSC Ensembl
Innerchr15:18845990..19399134hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38548424
hg19548500
hg18553145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047777
Supporting Variants
Samples
Known GenesCXADRP2, 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)nssv3537266
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer