A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628178



Internal ID21576483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99410376..99410376hg38UCSC Ensembl
chr7:99007999..99007999hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144341
SamplesHG00512
Known GenesBUD31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628178
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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