A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220436



Internal ID20787476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102099762..102109620hg38UCSC Ensembl
chr8:103111990..103121848hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg389859
hg199859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424741
Supporting Variants
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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