A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180924



Internal ID20747964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80219901..80260600hg38UCSC Ensembl
chr10:81979657..82020356hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3840700
hg1940700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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