A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633171



Internal ID21581476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92576378..92576378hg38UCSC Ensembl
chr7:92205692..92205692hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142116
SamplesHG03065
Known GenesFAM133B, FAM133DP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633171
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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