A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949463



Internal ID33653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67236926..67255842hg38UCSC Ensembl
chr4:68102644..68121560hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3818917
hg1918917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949463
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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