A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700322



Internal ID15436974
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 StatusS
Merged Variantsnsv524403
Supporting Variants
Samples
Known GenesFPR1, FPR2, FPR3, HAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700322
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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