A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080596



Internal ID20647636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161255501..161256900hg38UCSC Ensembl
chr2:162112012..162113411hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0013


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