A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951666



Internal ID35135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89680804..89681315hg38UCSC Ensembl
chr4:90601955..90602466hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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