A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530989



Internal ID306955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41930684..41931221hg38UCSC Ensembl
chr19:42434836..42435373hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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