A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489689



Internal ID21147242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109311395..109311547hg38UCSC Ensembl
chr13:109963743..109963895hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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