A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483889



Internal ID21141442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95284464..95382514hg38UCSC Ensembl
chr13:95936718..96034768hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3898051
hg1998051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178828
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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