A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213701



Internal ID20780741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4634409..4663415hg38UCSC Ensembl
chr4:4636136..4665142hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3829007
hg1929007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371038
Supporting Variants
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213701
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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