A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538282



Internal ID18489877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..22472558hg38UCSC Ensembl
Innerchr15:20216943..22751668hg19UCSC Ensembl
Innerchr15:18476957..20303032hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382460869
hg192534726
hg181826076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036304
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3538282
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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