A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441792



Internal ID22107973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92473119..92473119hg38UCSC Ensembl
chr12:92866895..92866895hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757426
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441792
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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