A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426176



Internal ID21083729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116872001..116876600hg38UCSC Ensembl
chr8:117884240..117888839hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218278
Samples
Known GenesMIR3610, RAD21, RAD21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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