A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088434



Internal ID21997667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8511029..8511029hg38UCSC Ensembl
chr17:8414347..8414347hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631329
Samples
Known GenesMYH10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088434
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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