A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990934



Internal ID20557974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40796936..40921176hg38UCSC Ensembl
chr11:40818486..40942726hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38124241
hg19124241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461564
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990934
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