A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526746



Internal ID15107353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4607575..4647219hg38UCSC Ensembl
Innerchr19:4607587..4647231hg19UCSC Ensembl
Innerchr19:4558587..4598231hg18UCSC Ensembl
Innerchr19:4558587..4598231hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3839645
hg1939645
hg1839645
hg1739645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703090
Samples
Known GenesTNFAIP8L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526746
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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