A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223096



Internal ID20790136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102136762..102137394hg38UCSC Ensembl
chr14:102603099..102603731hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581942
Supporting Variants
Samples
Known GenesHSP90AA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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