A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423643



Internal ID21081196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25306837..25307473hg38UCSC Ensembl
chr8:25164353..25164989hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167888
Samples
Known GenesDOCK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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