A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975100



Internal ID22750035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31937602..32149843hg38UCSC Ensembl
chr9:31937600..32149841hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38212242
hg19212242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440597
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975100
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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