A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183011



Internal ID20750051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97107601..97111500hg38UCSC Ensembl
chr13:97759855..97763754hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183011
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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