A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170783



Internal ID20737823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88910058..89092897hg38UCSC Ensembl
chr8:89922287..90105126hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38182840
hg19182840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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