A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422322



Internal ID21079875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90994201..90995500hg38UCSC Ensembl
chr8:92006429..92007728hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172732
Samples
Known GenesTMEM55A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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