A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701865



Internal ID21198443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66251546..66252426hg38UCSC Ensembl
chr11:66019017..66019897hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791093
Supporting Variants
SamplesCHM13
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701865
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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