A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604381



Internal ID21796428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30839252..30839609hg38UCSC Ensembl
chr13:31413389..31413746hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034139
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604381
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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