A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477283



Internal ID21134836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97355935..97424791hg38UCSC Ensembl
chr13:98008189..98077045hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3868857
hg1968857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193085
Samples
Known GenesMBNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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