A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579035



Internal ID20952106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131278557..131281792hg38UCSC Ensembl
chr10:133076820..133080055hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383236
hg193236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228148
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579035
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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