A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623558



Internal ID21571863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32537927..32537927hg38UCSC Ensembl
chr3:32579419..32579419hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122922
SamplesHG00512
Known GenesDYNC1LI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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