A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427068



Internal ID21084621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123862001..123864700hg38UCSC Ensembl
chr8:124874241..124876940hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225721
Samples
Known GenesFER1L6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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