A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585099



Internal ID20958170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12704218..12705858hg38UCSC Ensembl
chr12:12857152..12858792hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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