A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950121



Internal ID34100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56088761..56089592hg38UCSC Ensembl
chr4:56954927..56955758hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950121
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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