A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521295



Internal ID15448588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:169808074..169813745hg38UCSC Ensembl
Innerchr5:169235078..169240749hg19UCSC Ensembl
Innerchr5:169167656..169173327hg18UCSC Ensembl
Innerchr5:169167656..169173327hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385672
hg195672
hg185672
hg175672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697901
Samples
Known GenesDOCK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521295
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