A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934499



Internal ID22709826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65080026..65080087hg38UCSC Ensembl
chr17:63076144..63076205hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934499
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