A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181116



Internal ID20748156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61448301..61470400hg38UCSC Ensembl
chr13:62022434..62044533hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3822100
hg1922100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181116
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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