A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279292



Internal ID20488510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88578412..88578594hg38UCSC Ensembl
chr3:88627562..88627744hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279292
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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