A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208110



Internal ID20775150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208112439..208124272hg38UCSC Ensembl
chr2:208977163..208988996hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3811834
hg1911834
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347535
Supporting Variants
Samples
Known GenesCRYGD, LOC100507443
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208110
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