A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429218



Internal ID21086771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100511565..100514482hg38UCSC Ensembl
chr8:101523793..101526710hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382918
hg192918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161353
Samples
Known GenesANKRD46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429218
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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