A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899736



Internal ID602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240335255..240346175hg38UCSC Ensembl
chr1:240498555..240509475hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3810921
hg1910921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449584
Supporting Variants
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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