A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277944



Internal ID20487162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129640509..129640671hg38UCSC Ensembl
chr3:129359352..129359514hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277944
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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