A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529733



Internal ID305744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48479800..48479925hg38UCSC Ensembl
chr19:48983057..48983182hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723869
Samples
Known GenesCYTH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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