A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063545



Internal ID21491461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240184928..240184928hg38UCSC Ensembl
chr1:240348228..240348228hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622096
Supporting Variants
SamplesNA19238
Known GenesFMN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063545
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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