A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743225



Internal ID20519213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88419065..88430948hg38UCSC Ensembl
chr3:88468215..88480098hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3811884
hg1911884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743225
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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