A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062497



Internal ID21971730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53502122..53502122hg38UCSC Ensembl
chr4:54368289..54368289hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385980
hg195980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547769
Samples
Known GenesLNX1, LNX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062497
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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