A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949376



Internal ID33597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65794372..65795428hg38UCSC Ensembl
chr4:66660090..66661146hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381057
hg191057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949376
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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