A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587391



Internal ID20960462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57710765..57711287hg38UCSC Ensembl
chr12:58104548..58105070hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228859
Samples
Known GenesOS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587391
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