A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692579



Internal ID15082545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50822889..50918366hg38UCSC Ensembl
Innerchr15:51115086..51210563hg19UCSC Ensembl
Innerchr15:48902378..48997855hg18UCSC Ensembl
Innerchr15:48902378..48997855hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3895478
hg1995478
hg1895478
hg1795478
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)nssv692579
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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