A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038787



Internal ID19128006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19989473..20327352hg38UCSC Ensembl
Innerchr15:20194726..20532605hg19UCSC Ensembl
Innerchr15:18454740..18792619hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38337880
hg19337880
hg18337880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n100
Supporting Variantsnssv3534451
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)nsv1038787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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