A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458245



Internal ID21115798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95257164..95258483hg38UCSC Ensembl
chr11:94990328..94991647hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381320
hg191320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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