A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475695



Internal ID21133248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110088885..110111061hg38UCSC Ensembl
chr13:110741232..110763408hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3822177
hg1922177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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