A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634416



Internal ID21582721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100581327..100581327hg38UCSC Ensembl
chr8:101593555..101593555hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156770
SamplesHG02011
Known GenesSNX31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634416
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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