A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709380



Internal ID21198421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123976385..123993771hg38UCSC Ensembl
chr9:126738664..126756050hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3817387
hg1917387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819057
Supporting Variants
SamplesCHM13
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709380
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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