A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443426



Internal ID22109609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113024268..113032468hg38UCSC Ensembl
chr3:112743115..112751315hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg388201
hg198201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761491
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443426
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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