A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096810



Internal ID22006043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45579431..45579431hg38UCSC Ensembl
chr10:46074879..46074879hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590827
Samples
Known GenesMARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096810
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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