A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097941



Internal ID21407712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16632193..18073542hg38UCSC Ensembl
chr16:16726050..18167399hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381441350
hg191441350
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666478
Supporting Variants
SamplesHG00512
Known GenesXYLT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097941
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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