A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405000



Internal ID22462870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38879286..38886630hg38UCSC Ensembl
chr22:39275291..39282635hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387345
hg197345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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