A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526539



Internal ID15107146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70839740..70871447hg38UCSC Ensembl
Innerchr10:72599497..72631204hg19UCSC Ensembl
Innerchr10:72269503..72301210hg18UCSC Ensembl
Innerchr10:72269503..72301210hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3831708
hg1931708
hg1831708
hg1731708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702853
Samples
Known GenesSGPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526539
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