A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481423



Internal ID21138976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96318535..96355498hg38UCSC Ensembl
chr13:96970789..97007752hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3836964
hg1936964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195027
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481423
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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