A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214411



Internal ID20781451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99305370..99322613hg38UCSC Ensembl
chr4:100226527..100243770hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3817244
hg1917244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390158
Supporting Variants
Samples
Known GenesADH1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer