A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713567



Internal ID19011848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..20404354hg38UCSC Ensembl
Innerchr15:20440526..20609607hg19UCSC Ensembl
Innerchr15:18700540..18869621hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38169082
hg19169082
hg18169082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052991
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)nssv3713567
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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