A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516662



Internal ID15097269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129673458..129675983hg38UCSC Ensembl
Innerchr10:131471722..131474247hg19UCSC Ensembl
Innerchr10:131361712..131364237hg18UCSC Ensembl
Innerchr10:131361712..131364237hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382526
hg192526
hg182526
hg172526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690506, nssv669992
Samples
Known GenesMGMT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516662
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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