A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988188



Internal ID20555228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133629367..133632066hg38UCSC Ensembl
chr11:133499262..133501961hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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