A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181739



Internal ID20748779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58771885..58780661hg38UCSC Ensembl
chr13:59346019..59354795hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg388777
hg198777
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181739
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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