A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446697



Internal ID22112875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58470629..58470945hg38UCSC Ensembl
chr13:59044763..59045079hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763820
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446697
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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