A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489998



Internal ID21147551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73118119..73140113hg38UCSC Ensembl
chr13:73692256..73714250hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3821995
hg1921995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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