A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734559



Internal ID20510496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115633656..115634132hg38UCSC Ensembl
chr5:114969353..114969829hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734559
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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