A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483726



Internal ID21141279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53050981..53051361hg38UCSC Ensembl
chr13:53625116..53625496hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009755
Samples
Known GenesOLFM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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