A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525224



Internal ID15452517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:170074523..170083388hg38UCSC Ensembl
Innerchr5:169501527..169510392hg19UCSC Ensembl
Innerchr5:169434105..169442970hg18UCSC Ensembl
Innerchr5:169434105..169442970hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg388866
hg198866
hg188866
hg178866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701312
Samples
Known GenesDOCK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525224
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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