A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262081



Internal ID20471299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152047140..152047579hg38UCSC Ensembl
chr3:151764929..151765368hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262081
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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