A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749156



Internal ID20525185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59608483..59609215hg38UCSC Ensembl
chr3:59594209..59594941hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749156
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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