A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954281



Internal ID36848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98585381..98592100hg38UCSC Ensembl
chr4:99506532..99513251hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg386720
hg196720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457205
Supporting Variants
Samples
Known GenesTSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954281
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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