A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588930



Internal ID21537494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69409865..69409914hg38UCSC Ensembl
chr10:71169621..71169670hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071152
SamplesHG00731
Known GenesTACR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588930
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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