A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495106



Internal ID21152659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99381033..99395998hg38UCSC Ensembl
chr13:100033287..100048252hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3814966
hg1914966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189289
Samples
Known GenesMIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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