A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522611



Internal ID21846970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240207639..240207740hg38UCSC Ensembl
chr1:240370939..240371040hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982974
Supporting Variants
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522611
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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