A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991103



Internal ID21900446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124367971..124368334hg38UCSC Ensembl
chr3:124086818..124087181hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538261
Samples
Known GenesKALRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991103
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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