A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742220



Internal ID20518201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91319362..91321189hg38UCSC Ensembl
chr5:90615179..90617006hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742220
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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