A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628430



Internal ID21576735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:924160..924160hg38UCSC Ensembl
chr7:963796..963796hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143525
SamplesHG03125
Known GenesADAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628430
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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