A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614045



Internal ID21562350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56635273..56635273hg38UCSC Ensembl
chr1:57100946..57100946hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg382065
hg192065
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065648
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614045
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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