A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423121



Internal ID21080674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81048723..81054709hg38UCSC Ensembl
chr8:81960958..81966944hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385987
hg195987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171290
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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