A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911791



Internal ID22687006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44915324..44918966hg38UCSC Ensembl
chr10:45410772..45414414hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383643
hg193643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355373
Samples
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911791
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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