A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839364



Internal ID22614299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53468119..53471046hg38UCSC Ensembl
chr4:54334286..54337213hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495921
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839364
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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