A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445645



Internal ID22111822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92120376..92120376hg38UCSC Ensembl
chr14:92586720..92586720hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765781
Samples
Known GenesNDUFB1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445645
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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