A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523368



Internal ID15450661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69819234..69849566hg38UCSC Ensembl
Innerchr15:70111573..70141905hg19UCSC Ensembl
Innerchr15:67898627..67928959hg18UCSC Ensembl
Innerchr15:67898627..67928959hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3830333
hg1930333
hg1830333
hg1730333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699117
Samples
Known GenesLINC00593
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer