A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581669



Internal ID20954740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95081842..95082390hg38UCSC Ensembl
chr12:95475618..95476166hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225280
Samples
Known GenesFGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581669
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