A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231729



Internal ID20798769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10232787..10233192hg38UCSC Ensembl
chr12:10385386..10385791hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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