A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261993



Internal ID20471211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39480866..39480932hg38UCSC Ensembl
chr2:39708007..39708073hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749282
Supporting Variants
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261993
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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