A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736390



Internal ID20512338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178793853..178793925hg38UCSC Ensembl
chr5:178220854..178220926hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736390
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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