A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424513



Internal ID21082066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140593641..140594868hg38UCSC Ensembl
chr8:141603740..141604967hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167263
Samples
Known GenesAGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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