A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617531



Internal ID21809578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39221224..39221275hg38UCSC Ensembl
chr13:39795361..39795412hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617531
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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