A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277190



Internal ID20486408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143921924..143921977hg38UCSC Ensembl
chr2:144679491..144679544hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277190
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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