A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442896



Internal ID22109078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31689241..31689241hg38UCSC Ensembl
chr20:30277044..30277044hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761091
Samples
Known GenesBCL2L1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442896
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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