A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464832



Internal ID242703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53496543..53496604hg38UCSC Ensembl
chr4:54362710..54362771hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951050
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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