A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442823



Internal ID22109005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44510749..44510799hg38UCSC Ensembl
chr3:44552241..44552291hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764137
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442823
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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