A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434362



Internal ID21091915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114238892..114240396hg38UCSC Ensembl
chr8:115251121..115252625hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381505
hg191505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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