A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145325



Internal ID21452026
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 StatusS
Merged Variantsnsv5628728
Supporting Variants
SamplesHG01596
Known GenesOSBPL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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