A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428773



Internal ID21086326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100296501..100298800hg38UCSC Ensembl
chr8:101308729..101311028hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161344
Samples
Known GenesRNF19A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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