A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353478



Internal ID21011031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137529040..137529412hg38UCSC Ensembl
chr2:138286610..138286982hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077150
Samples
Known GenesTHSD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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