A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434886



Internal ID21092439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104392686..104406426hg38UCSC Ensembl
chr8:105404914..105418654hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3813741
hg1913741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162725
Samples
Known GenesDPYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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