A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169051



Internal ID20736091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54331862..54344497hg38UCSC Ensembl
chr8:55244422..55257057hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3812636
hg1912636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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