A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608983



Internal ID21801030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76828071..76828189hg38UCSC Ensembl
chr13:77402206..77402324hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608983
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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