A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489203



Internal ID21146756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51287081..51307831hg38UCSC Ensembl
chr13:51861217..51881967hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3820751
hg1920751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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