A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484407



Internal ID21141960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71226001..71284500hg38UCSC Ensembl
chr13:71800133..71858632hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3858500
hg1958500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1912n223
Supporting Variantsnssv18190230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484407
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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