A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467489



Internal ID21125042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77557448..77558003hg38UCSC Ensembl
chr11:77268493..77269048hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467489
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