A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609534



Internal ID21557839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26488458..26488458hg38UCSC Ensembl
chr1:26814949..26814949hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064311
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609534
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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