A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494767



Internal ID21152320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75535601..75546300hg38UCSC Ensembl
chr13:76109737..76120436hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n223
Supporting Variantsnssv18185928
Samples
Known GenesCOMMD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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