A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448357



Internal ID22114535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112732490..112732490hg38UCSC Ensembl
chr2:113490067..113490067hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759038
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448357
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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