A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458583



Internal ID21116136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106773501..106776500hg38UCSC Ensembl
chr11:106644227..106647226hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986104
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458583
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