A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185513



Internal ID20752553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71872048..71876946hg38UCSC Ensembl
chr10:73631806..73636704hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384899
hg194899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185513
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