A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286116



Internal ID22116805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14395904..14398047hg38UCSC Ensembl
chr19:14506716..14508859hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231050
Supporting Variants
SamplesHG00512
Known GenesCD97
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286116
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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