A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526529



Internal ID15107136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101580299..101594425hg38UCSC Ensembl
Innerchr10:103340056..103354182hg19UCSC Ensembl
Innerchr10:103330046..103344172hg18UCSC Ensembl
Innerchr10:103330046..103344172hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3814127
hg1914127
hg1814127
hg1714127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702842
Samples
Known GenesDPCD, POLL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526529
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