A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443789



Internal ID22109970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179650349..179650476hg38UCSC Ensembl
chr5:179077350..179077477hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764583
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443789
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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