A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583765



Internal ID20956836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:123593953..123594751hg38UCSC Ensembl
chr12:124078500..124079298hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225128
Samples
Known GenesTMED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583765
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