A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420370



Internal ID21077923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23225576..23227788hg38UCSC Ensembl
chr8:23083089..23085301hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382213
hg192213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232238
Samples
Known GenesLOC389641
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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