A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430599



Internal ID21088152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139720507..139722021hg38UCSC Ensembl
chr8:140732750..140734264hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381515
hg191515
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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