A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449267



Internal ID22115444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98356257..98356334hg38UCSC Ensembl
chr14:98822594..98822671hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756740
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449267
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer