A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432819



Internal ID21090372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119111201..119118900hg38UCSC Ensembl
chr8:120123440..120131139hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432819
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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