A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445608



Internal ID22111786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91836577..91836577hg38UCSC Ensembl
chr14:92302921..92302921hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767694
Samples
Known GenesTC2N
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445608
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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