A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170028



Internal ID20737068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:5921234..6172632hg38UCSC Ensembl
chr8:5778756..6030153hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38251399
hg19251398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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