A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611300



Internal ID21559605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203268404..203268404hg38UCSC Ensembl
chr1:203237532..203237532hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062583
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611300
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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