A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485346



Internal ID262737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11111884..11115051hg38UCSC Ensembl
chr10:11153847..11157014hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383168
hg193168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029129
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485346
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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