A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195077



Internal ID20762117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89067295..89277075hg38UCSC Ensembl
chr13:89719549..89929329hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38209781
hg19209781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195077
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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