A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493598



Internal ID21151151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28289762..28291711hg38UCSC Ensembl
chr13:28863899..28865848hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg381950
hg191950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008351
Samples
Known GenesPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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