A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537369



Internal ID18835650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22145275hg38UCSC Ensembl
Innerchr15:20585976..22433226hg19UCSC Ensembl
Innerchr15:18845990..19934590hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381764553
hg191847251
hg181088601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047402
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)nssv3537369
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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