A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525476



Internal ID15452769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57465261..57508411hg38UCSC Ensembl
Innerchr3:57450988..57494138hg19UCSC Ensembl
Innerchr3:57426028..57469178hg18UCSC Ensembl
Innerchr3:57426028..57469178hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3843151
hg1943151
hg1843151
hg1743151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv286n21
Supporting Variantsnssv701604
Samples
Known GenesDNAH12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525476
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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