A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444031



Internal ID22110213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111631288..111631288hg38UCSC Ensembl
chr13:112283635..112283635hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761660
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444031
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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