A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622909



Internal ID21571214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157760715..157760715hg38UCSC Ensembl
chr1:157730505..157730505hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061210
SamplesNA20847
Known GenesFCRL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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