A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287412



Internal ID20496630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113737245..113737245hg38UCSC Ensembl
chr13:114440218..114440218hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287412
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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