A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952561



Internal ID35731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81261390..81267234hg38UCSC Ensembl
chr4:82182544..82188388hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg385845
hg195845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952561
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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