A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583271



Internal ID20956342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9221365..9222267hg38UCSC Ensembl
chr12:9373961..9374863hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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