A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227141



Internal ID20794181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32999714..33009029hg38UCSC Ensembl
chr8:32857232..32866547hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389316
hg199316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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