A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626160



Internal ID21574465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101752957..101752957hg38UCSC Ensembl
chr8:102765185..102765185hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157198
SamplesNA19238
Known GenesNCALD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626160
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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