A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042342



Internal ID19131561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20336715hg38UCSC Ensembl
Innerchr15:20262224..20541968hg19UCSC Ensembl
Innerchr15:18522238..18801982hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38279745
hg19279745
hg18279745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3538284
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)nsv1042342
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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