A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486887



Internal ID21144440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19817842..19939076hg38UCSC Ensembl
chr13:20391982..20513216hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38121235
hg19121235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n223
Supporting Variantsnssv18194936
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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