A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426812



Internal ID21084365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:118068401..118079500hg38UCSC Ensembl
chr8:119080640..119091739hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3811100
hg1911100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224262
Samples
Known GenesEXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426812
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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