A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162826



Internal ID20729867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108901301..108902600hg38UCSC Ensembl
chr8:109913530..109914829hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432624
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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