A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182145



Internal ID20749185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77486938..77501111hg38UCSC Ensembl
chr13:78061073..78075246hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3814174
hg1914174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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