A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445648



Internal ID22111825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94345973..94345973hg38UCSC Ensembl
chr14:94812310..94812310hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760693
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445648
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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