A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944061



Internal ID21364130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115246540..115246540hg38UCSC Ensembl
chr10:117006327..117006327hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192151
SamplesHG002
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944061
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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