A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947145



Internal ID32124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35625821..35628470hg38UCSC Ensembl
chr4:35627443..35630092hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947145
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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