A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441967



Internal ID22108149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106209873..106209873hg38UCSC Ensembl
chr12:106603651..106603651hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767130
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441967
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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