A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427006



Internal ID21084559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142699801..142701600hg38UCSC Ensembl
chr8:143781219..143783018hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228349
Samples
Known GenesLY6K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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