A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522566



Internal ID8416841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43101280..43115223hg38UCSC Ensembl
Innerchr10:43596728..43610671hg19UCSC Ensembl
Innerchr10:42916734..42930677hg18UCSC Ensembl
Innerchr10:42916734..42930677hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813944
hg1913944
hg1813944
hg1713944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705950
Samples
Known GenesRET
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522566
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