A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652598



Internal ID15042564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41842103..41855441hg38UCSC Ensembl
Innerchr15:42134301..42147639hg19UCSC Ensembl
Innerchr15:39921593..39934931hg18UCSC Ensembl
Innerchr15:39921593..39934931hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3813339
hg1913339
hg1813339
hg1713339
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517631
Supporting Variants
Samples
Known GenesJMJD7-PLA2G4B, PLA2G4B, SPTBN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652598
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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