A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555280



Internal ID20928372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42085143..42088439hg38UCSC Ensembl
chr22:42481147..42484443hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074550
Samples
Known GenesNDUFA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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