A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261112



Internal ID20470330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31190136..31191075hg38UCSC Ensembl
chr5:31190243..31191182hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261112
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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