A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199077



Internal ID20766117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8677004..8710590hg38UCSC Ensembl
chr19:8786839..8820943hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3833587
hg1934105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526133
Supporting Variants
Samples
Known GenesACTL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199077
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