A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286678



Internal ID20495896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29555236..30655096hg38UCSC Ensembl
chr1:30028083..31127943hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg381099861
hg191099861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286678
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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