A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641645



Internal ID21589950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78711858..78711858hg38UCSC Ensembl
chr5:78007681..78007681hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146831
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641645
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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