A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231397



Internal ID20798437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14217921..14218869hg38UCSC Ensembl
chr10:14259920..14260868hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585609
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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