A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184323



Internal ID20751363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85298529..85328171hg38UCSC Ensembl
chr13:85872664..85902306hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3829643
hg1929643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184323
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