A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217820



Internal ID20784860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23669708..23670708hg38UCSC Ensembl
chr14:24138917..24139917hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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