A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178639



Internal ID20745679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87593772..87678825hg38UCSC Ensembl
chr12:87987549..88072602hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3885054
hg1985054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178639
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