A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077810



Internal ID21987043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108471071..108471071hg38UCSC Ensembl
chr3:108189918..108189918hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557463
Samples
Known GenesMYH15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077810
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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