A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993214



Internal ID20560254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62563058..62565021hg38UCSC Ensembl
chr11:62330530..62332493hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381964
hg191964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462780
Supporting Variants
Samples
Known GenesEEF1G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer