A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947007



Internal ID32030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22553078..22553934hg38UCSC Ensembl
chr4:22554701..22555557hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947007
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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