A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620497



Internal ID21568802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24975993..24975993hg38UCSC Ensembl
chr1:25302484..25302484hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064441
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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