A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235078



Internal ID20802118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101531884..101532739hg38UCSC Ensembl
chr12:101925662..101926517hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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