A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614014



Internal ID21806061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74570377..74570377hg38UCSC Ensembl
chr13:75144514..75144514hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614014
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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