A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713618



Internal ID19011899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20397153hg38UCSC Ensembl
Innerchr15:20446126..20602406hg19UCSC Ensembl
Innerchr15:18706140..18862420hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38156281
hg19156281
hg18156281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050855
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)nssv3713618
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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