A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275773



Internal ID20484991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154583447..154583565hg38UCSC Ensembl
chr5:153963007..153963125hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275773
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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