A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974635



Internal ID22749570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135170260..135232799hg38UCSC Ensembl
chr9:138062106..138124645hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3862540
hg1962540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436065
Samples
Known GenesLOC401557
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974635
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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