A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494974



Internal ID21152527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34982201..34986900hg38UCSC Ensembl
chr13:35556338..35561037hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1800n223
Supporting Variantsnssv18188182
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494974
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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