A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954911



Internal ID37252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109847487..109847608hg38UCSC Ensembl
chr4:110768643..110768764hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954911
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006088


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