A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682320



Internal ID15072286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41805538..41895294hg38UCSC Ensembl
Innerchr15:42097736..42187492hg19UCSC Ensembl
Innerchr15:39885028..39974784hg18UCSC Ensembl
Innerchr15:39885028..39974784hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3889757
hg1989757
hg1889757
hg1789757
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517631
Supporting Variants
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)nssv682320
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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