A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117414



Internal ID20684454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53461042..53461434hg38UCSC Ensembl
chr4:54327209..54327601hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395505
Supporting Variants
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00273


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer