A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444225



Internal ID22110405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160535699..160535842hg38UCSC Ensembl
chr2:161392210..161392353hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764534
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444225
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