A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588707



Internal ID20961778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121717812..121719145hg38UCSC Ensembl
chr10:123477326..123478659hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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