A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491791



Internal ID21149344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107311876..107324179hg38UCSC Ensembl
chr13:107964224..107976527hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3812304
hg1912304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189282
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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