A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089365



Internal ID20656405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46805907..46821451hg38UCSC Ensembl
chr2:47033046..47048590hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3815545
hg1915545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352405
Supporting Variants
Samples
Known GenesLINC01118
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089365
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