A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519726



Internal ID15447019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84654916..84724136hg38UCSC Ensembl
Innerchr10:86414672..86483892hg19UCSC Ensembl
Innerchr10:86404652..86473872hg18UCSC Ensembl
Innerchr10:86404652..86473872hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3869221
hg1969221
hg1869221
hg1769221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697014
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519726
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer