A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206047



Internal ID20773087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30063094..30102073hg38UCSC Ensembl
chr21:31435412..31474391hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3838980
hg1938980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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