A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538286



Internal ID18836567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20364686hg38UCSC Ensembl
Innerchr15:20262224..20569939hg19UCSC Ensembl
Innerchr15:18522238..18829953hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38307716
hg19307716
hg18307716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050283
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)nssv3538286
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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