A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432412



Internal ID21089965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123861201..123866300hg38UCSC Ensembl
chr8:124873441..124878540hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223049
Samples
Known GenesFER1L6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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