A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449154



Internal ID22115331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18096971..18096971hg38UCSC Ensembl
chr12:18249905..18249905hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756157
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449154
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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