A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971731



Internal ID48507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102671807..102677403hg38UCSC Ensembl
chr5:102007511..102013107hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg385597
hg195597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971731
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009654


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