A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203931



Internal ID20770971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35354789..35384333hg38UCSC Ensembl
chr21:36727087..36756631hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3829545
hg1929545
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554880
Supporting Variants
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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