A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523450



Internal ID15450743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36247246..36272710hg38UCSC Ensembl
Innerchr10:36536174..36561638hg19UCSC Ensembl
Innerchr10:36576180..36601644hg18UCSC Ensembl
Innerchr10:36576180..36601644hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3825465
hg1925465
hg1825465
hg1725465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699207
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523450
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