A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183203



Internal ID20750243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21450048..21471614hg38UCSC Ensembl
chr10:21738977..21760543hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3821567
hg1921567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183203
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