A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537596



Internal ID18835877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22129590hg38UCSC Ensembl
Innerchr15:20564575..22417541hg19UCSC Ensembl
Innerchr15:18824589..19918905hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381770269
hg191852967
hg181094317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051146
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, 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)nssv3537596
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