A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463976



Internal ID241865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53602844..53608612hg38UCSC Ensembl
chr4:54469011..54474779hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385769
hg195769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735094
Samples
Known GenesLNX1-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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