A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628513



Internal ID21576818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28973617..28973617hg38UCSC Ensembl
chr7:29013233..29013233hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148512
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628513
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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