A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433285



Internal ID21090838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82677801..82701000hg38UCSC Ensembl
chr8:83590036..83613235hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3823200
hg1923200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433285
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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