A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994151



Internal ID20561191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77593301..77600800hg38UCSC Ensembl
chr11:77304346..77311845hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464792
Supporting Variants
Samples
Known GenesAQP11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994151
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