A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203758



Internal ID20770798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14245507..14287612hg38UCSC Ensembl
chr21:15617828..15659933hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3842106
hg1942106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543111
Supporting Variants
Samples
Known GenesABCC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00033


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