A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485489



Internal ID21143042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68861785..68862389hg38UCSC Ensembl
chr13:69435917..69436521hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012167
Samples
Known GenesLINC00550
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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