A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609209



Internal ID21557514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58074564..58074564hg38UCSC Ensembl
chr1:58540236..58540236hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066013
SamplesHG00096
Known GenesDAB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609209
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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