A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517064



Internal ID15444357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121181867..121197234hg38UCSC Ensembl
Innerchr10:122941381..122956748hg19UCSC Ensembl
Innerchr10:122931371..122946738hg18UCSC Ensembl
Innerchr10:122931371..122946738hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3815368
hg1915368
hg1815368
hg1715368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674190, nssv689890, nssv653715, nssv670850, nssv673368, nssv665574, nssv657828, nssv685862, nssv667740, nssv690030
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517064
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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