A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431338



Internal ID21088891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79302620..79307834hg38UCSC Ensembl
chr8:80214855..80220069hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385215
hg195215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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