A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052232



Internal ID19141451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20406104hg38UCSC Ensembl
Innerchr15:20203949..20611357hg19UCSC Ensembl
Innerchr15:18463963..18871371hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38407409
hg19407409
hg18407409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2176n100
Supporting Variantsnssv3534498
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)nsv1052232
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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