A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078345



Internal ID20645385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145659794..145660740hg38UCSC Ensembl
chr2:146417362..146418308hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078345
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