A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052064



Internal ID19141283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20381692hg38UCSC Ensembl
Innerchr15:20284054..20586945hg19UCSC Ensembl
Innerchr15:18544068..18846959hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38302892
hg19302892
hg18302892
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2198n100
Supporting Variantsnssv3715975, nssv3540029, nssv3540028, nssv3715974
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)nsv1052064
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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