A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666589



Internal ID15056555
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 StatusS
Merged Variantsnsv516168
Supporting Variants
Samples
Known GenesAP4E1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666589
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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