A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563442



Internal ID336376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119782995..119792189hg38UCSC Ensembl
chr4:120704150..120713344hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg389195
hg199195
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563442
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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