A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422305



Internal ID21079858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92892601..92893800hg38UCSC Ensembl
chr8:93904829..93906028hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173498
Samples
Known GenesTRIQK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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