A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437099



Internal ID22103276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126074684..126074684hg38UCSC Ensembl
chr8:127086928..127086928hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756407
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437099
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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