A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739094



Internal ID20515066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32855870..32856975hg38UCSC Ensembl
chr5:32855976..32857081hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739094
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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