A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446042



Internal ID22112221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10278073..10278073hg38UCSC Ensembl
chr2:10418199..10418199hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767280
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446042
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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