A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759237



Internal ID20535097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55266342..55266342hg38UCSC Ensembl
chr19:55777710..55777710hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267142
Samples
Known GenesHSPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759237
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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