A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950209



Internal ID34158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62650474..62652224hg38UCSC Ensembl
chr4:63516192..63517942hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381751
hg191751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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