A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206413



Internal ID20773453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82281571..82351617hg38UCSC Ensembl
chr2:82508695..82578741hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3870047
hg1970047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206413
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