A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643439



Internal ID21591744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24917403..24917403hg38UCSC Ensembl
chr7:24957022..24957022hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150443
SamplesHG00512
Known GenesOSBPL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643439
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