A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949886



Internal ID22725325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53502122..53502122hg38UCSC Ensembl
chr4:54368289..54368289hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421249
Samples
Known GenesLNX1, LNX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949886
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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