A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219639



Internal ID20786679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95112275..95113231hg38UCSC Ensembl
chr12:95506051..95507007hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590832
Supporting Variants
Samples
Known GenesFGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219639
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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