A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079705



Internal ID20646745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164660901..164662000hg38UCSC Ensembl
chr2:165517411..165518510hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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