A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474289



Internal ID21131842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57521968..57526698hg38UCSC Ensembl
chr11:57289441..57294171hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384731
hg194731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474289
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