A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294374



Internal ID20503592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37215568..37215568hg38UCSC Ensembl
chr13:37789705..37789705hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767754
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294374
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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