A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037623



Internal ID19126842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20401433..20806746hg38UCSC Ensembl
Innerchr15:20606686..21012075hg19UCSC Ensembl
Innerchr15:18866700..19272115hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38405314
hg19405390
hg18405416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2257n100
Supporting Variantsnssv3540825
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)nsv1037623
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