A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228293



Internal ID20795333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21680218..21680965hg38UCSC Ensembl
chr10:21969147..21969894hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576103
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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