A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553845



Internal ID21878200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147690405..147691303hg38UCSC Ensembl
chr3:147408192..147409090hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553845
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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