A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226779



Internal ID20793819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32356231..32356598hg38UCSC Ensembl
chr12:32509165..32509532hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581393
Supporting Variants
Samples
Known GenesBICD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226779
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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