A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741857



Internal ID20517835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43998020..43998072hg38UCSC Ensembl
chr19:44502172..44502224hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263891
Samples
Known GenesZNF155
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741857
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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