A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993153



Internal ID21902496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21572322..21577235hg38UCSC Ensembl
chr3:21613814..21618727hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384914
hg194914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552783
Samples
Known GenesZNF385D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993153
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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