A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441389



Internal ID22107569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70407944..70407944hg38UCSC Ensembl
chr10:72167700..72167700hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762407
Samples
Known GenesEIF4EBP2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441389
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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