A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634098



Internal ID21582403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140706031..140706031hg38UCSC Ensembl
chr7:140405831..140405831hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147974
SamplesNA19239
Known GenesNDUFB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634098
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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