A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111483



Internal ID20678523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137998437..138085880hg38UCSC Ensembl
chr4:138919591..139007034hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3887444
hg1987444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384174
Supporting Variants
Samples
Known GenesLINC00616
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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