A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568765



Internal ID21517115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94659438..94659511hg38UCSC Ensembl
chr7:94288750..94288823hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153331
SamplesHG00513
Known GenesPEG10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568765
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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