A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992235



Internal ID20559275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48964118..49887182hg38UCSC Ensembl
chr11:48985670..49908734hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38923065
hg19923065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457045
Supporting Variants
Samples
Known GenesFOLH1, LOC440040, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992235
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