A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992219



Internal ID21901562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187714221..187714395hg38UCSC Ensembl
chr3:187432009..187432183hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552277
Samples
Known GenesLOC100131635
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992219
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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