A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518035



Internal ID15445328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:200355035..200395745hg38UCSC Ensembl
Innerchr1:200324163..200364873hg19UCSC Ensembl
Innerchr1:198590786..198631496hg18UCSC Ensembl
Innerchr1:197055820..197096530hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3840711
hg1940711
hg1840711
hg1740711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695445
Samples
Known GenesLINC00862
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518035
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