A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014376



Internal ID21923719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89302510..89302662hg38UCSC Ensembl
chr10:91062267..91062419hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594655
Samples
Known GenesIFIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014376
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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