A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530682



Internal ID306654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34423474..34423765hg38UCSC Ensembl
chr19:34914379..34914670hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722943
Samples
Known GenesPDCD2L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530682
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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