A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608845



Internal ID21557150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244167872..244167872hg38UCSC Ensembl
chr1:244331174..244331174hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063682
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608845
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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