A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610372



Internal ID21558677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206523627..206523627hg38UCSC Ensembl
chr1:206696960..206696960hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062762
SamplesHG03009
Known GenesRASSF5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610372
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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