A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186321



Internal ID20753362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22031339..22561000hg38UCSC Ensembl
chr11:22052885..22582546hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38529662
hg19529662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451445
Supporting Variants
Samples
Known GenesANO5, SLC17A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186321
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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