A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620561



Internal ID21568866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40030772..40030772hg38UCSC Ensembl
chr1:40496444..40496444hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065233
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620561
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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