A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518200



Internal ID15445493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55163699..55190498hg38UCSC Ensembl
Innerchr13:55737834..55764633hg19UCSC Ensembl
Innerchr13:54635835..54662634hg18UCSC Ensembl
Innerchr13:54635835..54662634hg17UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3826800
hg1926800
hg1826800
hg1726800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695623
Samples
Known GenesMIR5007
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518200
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