A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112088



Internal ID20679128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138412780..138435565hg38UCSC Ensembl
chr4:139333934..139356719hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3822786
hg1922786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389021
Supporting Variants
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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