A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749849



Internal ID20525884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43783117..43794425hg38UCSC Ensembl
chr5:43783219..43794527hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3811309
hg1911309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749849
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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