A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732609



Internal ID20508533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31867304..31867363hg38UCSC Ensembl
chr13:32441441..32441500hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274757
Samples
Known GenesEEF1DP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732609
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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