A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991079



Internal ID20558119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40328675..40329992hg38UCSC Ensembl
chr11:40350225..40351542hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381318
hg191318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461481
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991079
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