A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224595



Internal ID20791635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56435959..56437016hg38UCSC Ensembl
chr12:56829743..56830800hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591055
Supporting Variants
Samples
Known GenesTIMELESS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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