A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591479



Internal ID20964550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50024378..50153422hg38UCSC Ensembl
chr10:51784138..51913182hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38129045
hg19129045
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv737n223
Supporting Variantsnssv18222765
Samples
Known GenesFAM21A, FAM21B, FLJ31813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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