A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634361



Internal ID21582666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116638610..116638610hg38UCSC Ensembl
chr7:116278664..116278664hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147415
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634361
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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