A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162251



Internal ID20729291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105129978..105130517hg38UCSC Ensembl
chr8:106142206..106142745hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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