A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522062



Internal ID15102669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16670509..16679857hg38UCSC Ensembl
Innerchr5:16670618..16679966hg19UCSC Ensembl
Innerchr5:16723618..16732966hg18UCSC Ensembl
Innerchr5:16723618..16732966hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg389349
hg199349
hg189349
hg179349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694126
Samples
Known GenesMYO10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522062
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