A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418944



Internal ID21076497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73892322..73900224hg38UCSC Ensembl
chr8:74804557..74812459hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg387903
hg197903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418944
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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