A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484959



Internal ID21142512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28274850..28275462hg38UCSC Ensembl
chr13:28848987..28849599hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007545
Samples
Known GenesPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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