A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086155



Internal ID20653195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220226401..220230500hg38UCSC Ensembl
chr2:221091122..221095221hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086155
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