A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170363



Internal ID20737403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73356146..73361242hg38UCSC Ensembl
chr8:74268381..74273477hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385097
hg195097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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