A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991984



Internal ID21901327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172767213..172767301hg38UCSC Ensembl
chr3:172485003..172485091hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548567
Samples
Known GenesECT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991984
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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