A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602484



Internal ID21794531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44277449..44277449hg38UCSC Ensembl
chr13:44851585..44851585hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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