A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987002



Internal ID20554042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115399219..115399665hg38UCSC Ensembl
chr11:115269937..115270383hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474921
Supporting Variants
Samples
Known GenesCADM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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