A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538244



Internal ID21862599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41306208..41306356hg38UCSC Ensembl
chr3:41347699..41347847hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993849
Supporting Variants
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538244
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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