A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434218



Internal ID21091771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58653529..58697276hg38UCSC Ensembl
chr8:59566088..59609835hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843748
hg1943748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234841
Samples
Known GenesNSMAF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434218
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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