A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615245



Internal ID21563550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180656443..180656443hg38UCSC Ensembl
chr1:180625579..180625579hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061438
SamplesHG03065
Known GenesXPR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615245
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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