A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536922



Internal ID18835203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20384895hg38UCSC Ensembl
Innerchr15:20216943..20590148hg19UCSC Ensembl
Innerchr15:18476957..18850162hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38373206
hg19373206
hg18373206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046162
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)nssv3536922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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