A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525229



Internal ID15105836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3123124..3127579hg38UCSC Ensembl
Innerchr10:3165316..3169771hg19UCSC Ensembl
Innerchr10:3155316..3159771hg18UCSC Ensembl
Innerchr10:3155316..3159771hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg384456
hg194456
hg184456
hg174456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701318
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525229
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