A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190746



Internal ID20757786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100065566..100072056hg38UCSC Ensembl
chr13:100717820..100724310hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg386491
hg196491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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