A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550977



Internal ID21875332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87855847..87857894hg38UCSC Ensembl
chr5:87151664..87153711hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550977
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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