A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061210



Internal ID21509885
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 StatusS
Merged Variantsnsv5622909
Supporting Variants
SamplesNA20847
Known GenesFCRL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061210
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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