A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545845



Internal ID21870200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120124306..120125092hg38UCSC Ensembl
chr3:119843153..119843939hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545845
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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