A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517631



Internal ID15098238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41804728..41895294hg38UCSC Ensembl
Innerchr15:42096926..42187492hg19UCSC Ensembl
Innerchr15:39884218..39974784hg18UCSC Ensembl
Innerchr15:39884218..39974784hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3890567
hg1990567
hg1890567
hg1790567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652598, nssv682320, nssv672157, nssv677235, nssv679020, nssv690496, nssv686868, nssv659851
Samples
Known GenesJMJD7, JMJD7-PLA2G4B, MAPKBP1, MIR4310, PLA2G4B, SPTBN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517631
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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