A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631478



Internal ID21579783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5549035..5549035hg38UCSC Ensembl
chr7:5588666..5588666hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141276
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631478
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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