A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3250183



Internal ID22377463
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291265, nssv14291264
SamplesHG00732, HG00733
Known GenesC19orf71, MFSD12
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3250183
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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