A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575380



Internal ID21523809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39334571..39334697hg38UCSC Ensembl
chr5:39334673..39334799hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138655
SamplesNA20509
Known GenesC9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575380
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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