A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058945



Internal ID21968178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55266319..55266676hg38UCSC Ensembl
chr19:55777687..55778044hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618878
Samples
Known GenesHSPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058945
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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