A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081816



Internal ID21991049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72594388..72594388hg38UCSC Ensembl
chr10:74354146..74354146hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588177
Samples
Known GenesMICU1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081816
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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