A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167937



Internal ID20734977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26432006..26433035hg38UCSC Ensembl
chr8:26289522..26290551hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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