A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538029



Internal ID20911355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32414124..32423129hg38UCSC Ensembl
chr22:32810111..32819116hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg389006
hg199006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073782
Samples
Known GenesBPIFC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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