A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449159



Internal ID22115336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26345014..26345065hg38UCSC Ensembl
chr1:26671505..26671556hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766589
Samples
Known GenesAIM1L
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449159
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