A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576227



Internal ID20949298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68437563..68438003hg38UCSC Ensembl
chr10:70197320..70197760hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237023
Samples
Known GenesDNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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