A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089987



Internal ID20657027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65670229..65672439hg38UCSC Ensembl
chr2:65897363..65899573hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382211
hg192211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6338298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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