A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440116



Internal ID22106294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51293959..51294231hg38UCSC Ensembl
chr15:51586156..51586428hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760424
Samples
Known GenesCYP19A1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440116
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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