A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536928



Internal ID18835209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20406244hg38UCSC Ensembl
Innerchr15:20216943..20611497hg19UCSC Ensembl
Innerchr15:18476957..18871511hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38394555
hg19394555
hg18394555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044314
Supporting Variants
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536928
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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