A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734124



Internal ID20510058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51212633..51213138hg38UCSC Ensembl
chr5:50508467..50508972hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734124
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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