A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492900



Internal ID21150453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93116501..93118100hg38UCSC Ensembl
chr13:93768754..93770353hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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