A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589689



Internal ID20962760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26140529..26141010hg38UCSC Ensembl
chr10:26429458..26429939hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220198
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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