A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516168



Internal ID15096775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50822240..50925164hg38UCSC Ensembl
Innerchr15:51114437..51217361hg19UCSC Ensembl
Innerchr15:48901729..49004653hg18UCSC Ensembl
Innerchr15:48901729..49004653hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38102925
hg19102925
hg18102925
hg17102925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692579, nssv666589
Samples
Known GenesAP4E1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516168
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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