A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234534



Internal ID20801574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102565119..102567532hg38UCSC Ensembl
chr8:103577347..103579760hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428095
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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