A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724065



Internal ID147731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50054874..50091150hg38UCSC Ensembl
chr19:50558131..50594407hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3836277
hg1936277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146371
Supporting Variants
Samples
Known GenesFLJ26850
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724065
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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