A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642721



Internal ID21591026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102640623..102640623hg38UCSC Ensembl
chr8:103652851..103652851hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140704
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642721
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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