A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546149



Internal ID20919368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49899290..49915372hg38UCSC Ensembl
chr22:50292938..50309020hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3816083
hg1916083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205711
Samples
Known GenesALG12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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