A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464488



Internal ID21122041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56969523..57004001hg38UCSC Ensembl
chr11:56736998..56771476hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3834479
hg1934479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178983
Samples
Known GenesOR5AK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464488
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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