A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759574



Internal ID20535434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32855870..32855870hg38UCSC Ensembl
chr5:32855976..32855976hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759574
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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