A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970603



Internal ID22745538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122761784..123114887hg38UCSC Ensembl
chr9:125524063..125877166hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38353104
hg19353104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435223
Samples
Known GenesGPR21, MIR600, MIR600HG, OR1K1, OR5C1, PDCL, RABGAP1, RC3H2, SNORD90, ZBTB26, ZBTB6
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970603
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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