A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436658



Internal ID215269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29939940..29949323hg38UCSC Ensembl
chr4:29941562..29950945hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg389384
hg199384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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