A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431469



Internal ID21089022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94789879..94790274hg38UCSC Ensembl
chr8:95802107..95802502hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171827
Samples
Known GenesDPY19L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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