A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738560



Internal ID20514530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159050149..159050220hg38UCSC Ensembl
chr5:158477157..158477228hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293408
Samples
Known GenesEBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738560
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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