A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486978



Internal ID21144531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98305508..98314366hg38UCSC Ensembl
chr13:98957762..98966620hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388859
hg198859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016359
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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