A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921277



Internal ID22696500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122200380..122201033hg38UCSC Ensembl
chr10:123959895..123960548hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355173
Samples
Known GenesTACC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921277
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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