A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268344



Internal ID20477562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102694499..102694499hg38UCSC Ensembl
chr13:103346849..103346849hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758383
Supporting Variants
Samples
Known GenesMETTL21C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268344
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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