A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420475



Internal ID21078028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120724595..120728282hg38UCSC Ensembl
chr8:121736835..121740522hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg383688
hg193688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164255
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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