A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748394



Internal ID20524419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93583271..93583332hg38UCSC Ensembl
chr5:92918977..92919038hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748394
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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