A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422363



Internal ID21079916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60651401..60652700hg38UCSC Ensembl
chr8:61563960..61565259hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422363
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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