A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544314



Internal ID21868669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161078655..161083521hg38UCSC Ensembl
chr3:160796443..160801309hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg384867
hg194867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544314
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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