A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533028



Internal ID308926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34934174..34934297hg38UCSC Ensembl
chr19:35425078..35425201hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722981
Samples
Known GenesZNF30
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533028
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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