A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518996



Internal ID15446289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39408349..39504492hg38UCSC Ensembl
Innerchr18:36988313..37084456hg19UCSC Ensembl
Innerchr18:35242311..35338454hg18UCSC Ensembl
Innerchr18:35242311..35338454hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3896144
hg1996144
hg1896144
hg1796144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696463
Samples
Known GenesLINC00669
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518996
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