A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537401



Internal ID20910734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47078505..47109593hg38UCSC Ensembl
chr22:47474401..47505489hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3831089
hg1931089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075019
Samples
Known GenesTBC1D22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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