A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460724



Internal ID21118277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36623222..36623843hg38UCSC Ensembl
chr11:36644772..36645393hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989927
Samples
Known GenesC11orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460724
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