A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210500



Internal ID20777540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30780397..30797000hg38UCSC Ensembl
chr3:30821889..30838492hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3816604
hg1916604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371388
Supporting Variants
Samples
Known GenesGADL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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