A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449232



Internal ID22115409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6985441..6985441hg38UCSC Ensembl
chr12:7094601..7094601hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761432
Samples
Known GenesLPCAT3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449232
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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