A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578205



Internal ID21526669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65083992..65085461hg38UCSC Ensembl
chr5:64379819..64381288hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381470
hg191470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151071
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578205
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