A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561956



Internal ID334922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19016842..19016842hg38UCSC Ensembl
chr19:19127651..19127651hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722069
Samples
Known GenesSUGP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561956
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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