A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957547



Internal ID39008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139416585..139417329hg38UCSC Ensembl
chr4:140337739..140338483hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957547
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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