A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524403



Internal ID15451696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51722514..51853538hg38UCSC Ensembl
Innerchr19:52225767..52356791hg19UCSC Ensembl
Innerchr19:56917579..57048603hg18UCSC Ensembl
Innerchr19:56917579..57048603hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38131025
hg19131025
hg18131025
hg17131025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700322
Samples
Known GenesFPR1, FPR2, FPR3, HAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524403
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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