A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476931



Internal ID21134484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98183484..98185893hg38UCSC Ensembl
chr13:98835738..98838147hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg382410
hg192410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016354
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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