A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987619



Internal ID20554660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122131800..122132885hg38UCSC Ensembl
chr11:122002508..122003593hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459038
Supporting Variants
Samples
Known GenesMIR100HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987619
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