A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750028



Internal ID20526063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160233050..160233123hg38UCSC Ensembl
chr5:159660057..159660130hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296281
Samples
Known GenesFABP6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750028
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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