A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476273



Internal ID21133826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109895488..109905995hg38UCSC Ensembl
chr13:110547835..110558342hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3810508
hg1910508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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