A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577911



Internal ID20950982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14668296..14669184hg38UCSC Ensembl
chr10:14710295..14711183hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231274
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577911
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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