A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098142



Internal ID21429997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10002..139264hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38129263
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665167
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098142
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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