A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587364



Internal ID20960435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94354495..94354863hg38UCSC Ensembl
chr12:94748271..94748639hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232703
Samples
Known GenesCCDC41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587364
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