A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210841



Internal ID20777881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135911917..135917932hg38UCSC Ensembl
chr4:136833072..136839087hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381904
Supporting Variants
Samples
Known GenesLINC00613
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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