A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417103



Internal ID22474973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53506856..53506856hg38UCSC Ensembl
chr4:54373023..54373023hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966061
Supporting Variants
Samples
Known GenesLNX1, LNX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417103
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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