A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620756



Internal ID21812803
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 StatusS
Merged Variantsnsv6050897
Supporting Variants
Samples
Known GenesZNF155
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620756
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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