A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050897



Internal ID21960131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43998012..43998065hg38UCSC Ensembl
chr19:44502164..44502217hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620756
Samples
Known GenesZNF155
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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