A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586692



Internal ID20959763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119151296..119151756hg38UCSC Ensembl
chr10:120910808..120911268hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227742
Samples
Known GenesSFXN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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