A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892144



Internal ID22667189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53602844..53608611hg38UCSC Ensembl
chr4:54469011..54474778hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385768
hg195768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420864
Samples
Known GenesLNX1-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892144
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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