A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183971



Internal ID20751011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66121279..66132249hg38UCSC Ensembl
chr15:66413617..66424587hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810971
hg1910971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506730
Supporting Variants
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183971
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