A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947669



Internal ID32473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7966604..7966675hg38UCSC Ensembl
chr4:7968331..7968402hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451799
Supporting Variants
Samples
Known GenesABLIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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