A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992209



Internal ID21901552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186486400..186486524hg38UCSC Ensembl
chr3:186204189..186204313hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556382
Samples
Known GenesLOC253573
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992209
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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