A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452613



Internal ID230761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201024494..201024550hg38UCSC Ensembl
chr2:201889217..201889273hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922874
Samples
Known GenesFAM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452613
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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