A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967788



Internal ID22742724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46899171..47068433hg38UCSC Ensembl
chr1:47364843..47534105hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38169263
hg19169263
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369699
Samples
Known GenesCYP4A11, CYP4X1, CYP4Z1, CYP4Z2P
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967788
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer