A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3535729



Internal ID18834010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20368893hg38UCSC Ensembl
Innerchr15:20216943..20574146hg19UCSC Ensembl
Innerchr15:18476957..18834160hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38357204
hg19357204
hg18357204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049884
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)nssv3535729
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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