A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478834



Internal ID21136387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88818142..88947037hg38UCSC Ensembl
chr13:89470396..89599291hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38128896
hg19128896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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