A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992439



Internal ID20559479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59367217..59367922hg38UCSC Ensembl
chr11:59134690..59135395hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456622
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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