A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012160



Internal ID21921503
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 Variantsnssv17584241
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012160
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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