A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487605



Internal ID21145158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86801454..86856485hg38UCSC Ensembl
chr13:87453709..87508740hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3855032
hg1955032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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