A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162476



Internal ID20729516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102157789..102161294hg38UCSC Ensembl
chr8:103170017..103173522hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg383506
hg193506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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