A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439897



Internal ID22106074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17349132..17349226hg38UCSC Ensembl
chr19:17459941..17460035hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763686
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439897
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