A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610449



Internal ID21802496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39285970..39285970hg38UCSC Ensembl
chr13:39860107..39860107hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610449
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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