A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628728



Internal ID21577033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24979839..24979839hg38UCSC Ensembl
chr7:25019458..25019458hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145325
SamplesHG01596
Known GenesOSBPL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628728
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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