A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819057



Internal ID21264395
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 StatusM
Merged Variants
Supporting Variantsnssv13709380
SamplesCHM13
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819057
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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