A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209531



Internal ID20776571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110932101..110959100hg38UCSC Ensembl
chr4:111853257..111880256hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3827000
hg1927000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209531
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