A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622497



Internal ID21570802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157548334..157548334hg38UCSC Ensembl
chr1:157518124..157518124hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg386116
hg196116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061205
SamplesNA19239
Known GenesFCRL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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