A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589136



Internal ID20962207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112828561..112829329hg38UCSC Ensembl
chr10:114588320..114589088hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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