A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231904



Internal ID20798944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:459469..459992hg38UCSC Ensembl
chr7:499106..499629hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.2096


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