A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659851



Internal ID15049817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41842103..41876202hg38UCSC Ensembl
Innerchr15:42134301..42168400hg19UCSC Ensembl
Innerchr15:39921593..39955692hg18UCSC Ensembl
Innerchr15:39921593..39955692hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3834100
hg1934100
hg1834100
hg1734100
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517631
Supporting Variants
Samples
Known GenesJMJD7-PLA2G4B, MIR4310, PLA2G4B, SPTBN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659851
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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