A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590272



Internal ID20963343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109698758..109699428hg38UCSC Ensembl
chr12:110136563..110137233hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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