A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216674



Internal ID20783714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154978663..154993645hg38UCSC Ensembl
chr6:155299797..155314779hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3814983
hg1914983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216674
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