A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445667



Internal ID22111844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113642117..113642179hg38UCSC Ensembl
chr12:114079922..114079984hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756877
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445667
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