A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577406



Internal ID20950477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94550469..94550807hg38UCSC Ensembl
chr10:96310226..96310564hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227007
Samples
Known GenesHELLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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