A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281104



Internal ID20490322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107827022..107827236hg38UCSC Ensembl
chr5:107162723..107162937hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281104
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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