A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927486



Internal ID22702714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25185361..25226455hg38UCSC Ensembl
chr8:25042876..25083971hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3841095
hg1941096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444093
Samples
Known GenesDOCK5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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