A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444792



Internal ID22110972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18925748..18925748hg38UCSC Ensembl
chr1:19252242..19252242hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761982
Samples
Known GenesIFFO2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444792
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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