A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591674



Internal ID20964745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100952706..100953169hg38UCSC Ensembl
chr10:102712463..102712926hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230428
Samples
Known GenesFAM178A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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