A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458625



Internal ID21116178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106789601..106791200hg38UCSC Ensembl
chr11:106660327..106661926hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986477
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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