A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582693



Internal ID20955764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92238421..92238875hg38UCSC Ensembl
chr12:92632197..92632651hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582693
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