A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069055



Internal ID21512703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132800266..132891417hg38UCSC Ensembl
chr10:134613770..134704921hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3891152
hg1991152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666606
Supporting Variants
Samples
Known GenesTTC40
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069055
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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