A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415761



Internal ID21073314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117243736..117255406hg38UCSC Ensembl
chr8:118255975..118267645hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3811671
hg1911671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415761
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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