A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536189



Internal ID18834470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..22032488hg38UCSC Ensembl
Innerchr15:20532605..22320439hg19UCSC Ensembl
Innerchr15:18792619..19821803hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381705137
hg191787835
hg181029185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044164
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, 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)nssv3536189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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