A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736092



Internal ID20512037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2862397..2863001hg38UCSC Ensembl
chr5:2862511..2863115hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736092
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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