A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236014



Internal ID20803054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50485307..50485736hg38UCSC Ensembl
chr12:50879090..50879519hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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