A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992482



Internal ID20559522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60093427..60115827hg38UCSC Ensembl
chr11:59860900..59883300hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3822401
hg1922401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467242
Supporting Variants
Samples
Known GenesMS4A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992482
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