A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633332



Internal ID21581637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107230013..107230013hg38UCSC Ensembl
chr7:106870458..106870458hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140237
SamplesNA20509
Known GenesCOG5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633332
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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