A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015287



Internal ID21924630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44879277..44882727hg38UCSC Ensembl
chr10:45374725..45378175hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383451
hg193451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579979
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015287
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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