A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291265



Internal ID22231675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3540927..3541581hg38UCSC Ensembl
chr19:3540925..3541579hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3250183
Supporting Variants
SamplesHG00733
Known GenesC19orf71, MFSD12
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291265
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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