A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613251



Internal ID21805298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31867309..31867379hg38UCSC Ensembl
chr13:32441446..32441516hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035092
Supporting Variants
Samples
Known GenesEEF1DP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613251
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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