A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990969



Internal ID21900312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113046673..113046727hg38UCSC Ensembl
chr3:112765520..112765574hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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