A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741655



Internal ID20517632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55202668..55202736hg38UCSC Ensembl
chr5:54498496..54498564hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741655
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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