A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738728



Internal ID20514699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108952539..108952623hg38UCSC Ensembl
chr5:108288240..108288324hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259372
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738728
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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