A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519533



Internal ID15446826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19678719..19720735hg38UCSC Ensembl
Innerchr19:19789528..19831544hg19UCSC Ensembl
Innerchr19:19650528..19692544hg18UCSC Ensembl
Innerchr19:19650528..19692544hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3842017
hg1942017
hg1842017
hg1742017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696905
Samples
Known GenesZNF101, ZNF14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519533
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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