A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227742



Internal ID20794782
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 StatusS
Merged Variantsnsv6586692
Supporting Variants
Samples
Known GenesSFXN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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