A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042840



Internal ID21952152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58411413..58411470hg38UCSC Ensembl
chr19:58922780..58922837hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626330
Samples
Known GenesZNF584
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042840
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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