A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927630



Internal ID22702859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79844600..79844837hg38UCSC Ensembl
chr17:77818399..77818636hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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