A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536264



Internal ID20909617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42097699..42101321hg38UCSC Ensembl
chr22:42493703..42497325hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg383623
hg193623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074551
Samples
Known GenesNDUFA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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