A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594238



Internal ID20967309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30658906..30659296hg38UCSC Ensembl
chr12:30811840..30812230hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224168
Samples
Known GenesIPO8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594238
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