A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626229



Internal ID21574534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67227410..67227410hg38UCSC Ensembl
chr5:66523238..66523238hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151520
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626229
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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