A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228159



Internal ID20795199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95117452..95118028hg38UCSC Ensembl
chr12:95511228..95511804hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595244
Supporting Variants
Samples
Known GenesFGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228159
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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