A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970771



Internal ID22745706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4623729..4661951hg38UCSC Ensembl
chr17:4527024..4565246hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3838223
hg1938223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373302
Samples
Known GenesALOX15
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970771
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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