A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586016



Internal ID20959087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10905307..10906529hg38UCSC Ensembl
chr12:11057906..11059128hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235437
Samples
Known GenesPRH1-PRR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586016
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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