A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035092



Internal ID21944435
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 StatusM
Merged Variants
Supporting Variantsnssv17613251
Samples
Known GenesEEF1DP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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