A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536361



Internal ID18834642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..22256018hg38UCSC Ensembl
Innerchr15:20556430..22543969hg19UCSC Ensembl
Innerchr15:18816444..20045333hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381904842
hg191987540
hg181228890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050631
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)nssv3536361
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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