A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045393



Internal ID18787924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19419312..19787121hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg18367810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3716148
Samples
Known GenesCT60, LOC727924
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045393
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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