A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745014



Internal ID20521018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154101068..154101134hg38UCSC Ensembl
chr5:153480628..153480694hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745014
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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