A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594196



Internal ID20967267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28271600..28280923hg38UCSC Ensembl
chr12:28424533..28433856hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg389324
hg199324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224699
Samples
Known GenesCCDC91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer