A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281757



Internal ID20490975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10507913..10507964hg38UCSC Ensembl
chr3:10549597..10549648hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281757
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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