A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715883



Internal ID19014164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..22122906hg38UCSC Ensembl
Innerchr15:20262224..22410857hg19UCSC Ensembl
Innerchr15:18522238..19912221hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382065936
hg192148634
hg181389984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054154
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, 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)nssv3715883
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