A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698397



Internal ID21198448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38769343..38793389hg38UCSC Ensembl
chr19:39259983..39284029hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3824047
hg1924047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799867
Supporting Variants
SamplesCHM13
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698397
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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