A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620536



Internal ID21568841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41369871..41369871hg38UCSC Ensembl
chr1:41835543..41835543hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065751
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620536
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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