A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953394



Internal ID36282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102078208..102129278hg38UCSC Ensembl
chr4:102999365..103050435hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3851071
hg1951071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953394
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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