A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466580



Internal ID21124133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46277601..46278200hg38UCSC Ensembl
chr11:46299152..46299751hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991762
Samples
Known GenesCREB3L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466580
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