A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205313



Internal ID20772353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181724421..181871606hg38UCSC Ensembl
chr2:182589148..182736333hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38147186
hg19147186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354209
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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