A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170503



Internal ID20737543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66984233..66987883hg38UCSC Ensembl
chr8:67896468..67900118hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg383651
hg193651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170503
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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