A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440588



Internal ID22106766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691047..68691343hg38UCSC Ensembl
chr15:68983386..68983682hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15755869
Samples
Known GenesCORO2B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440588
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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