A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423913



Internal ID21081466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122349950..122350941hg38UCSC Ensembl
chr8:123362189..123363180hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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