A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635309



Internal ID21583614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23004130..23004130hg38UCSC Ensembl
chr10:23293059..23293059hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068117
SamplesHG03125
Known GenesARMC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635309
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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