A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988064



Internal ID20555104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132817054..132817362hg38UCSC Ensembl
chr11:132686949..132687257hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464770
Supporting Variants
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00144


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