A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554916



Internal ID20928006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151239641..151240995hg38UCSC Ensembl
chr1:151212117..151213471hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248141
Samples
Known GenesPIP5K1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554916
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