A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043521



Internal ID21952815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12292301..12294048hg38UCSC Ensembl
chr19:12403116..12404863hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636630
Samples
Known GenesZNF44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043521
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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