A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993720



Internal ID21903063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71782844..71782924hg38UCSC Ensembl
chr3:71831995..71832075hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543473
Samples
Known GenesPROK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993720
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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