A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429314



Internal ID21086867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123714740..123717424hg38UCSC Ensembl
chr8:124726980..124729664hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382685
hg192685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164019
Samples
Known GenesANXA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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