A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482696



Internal ID21140249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104687350..104697852hg38UCSC Ensembl
chr13:105339701..105350203hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3810503
hg1910503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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