A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474426



Internal ID21131979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65399257..65409333hg38UCSC Ensembl
chr11:65166728..65176804hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810077
hg1910077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994115
Samples
Known GenesFRMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474426
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