A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218378



Internal ID20785418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57711158..57711362hg38UCSC Ensembl
chr12:58104941..58105145hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592132
Supporting Variants
Samples
Known GenesOS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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