A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611321



Internal ID21559626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207407383..207407383hg38UCSC Ensembl
chr1:207580728..207580728hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062471
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611321
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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