A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238729



Internal ID22374239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163216749..163236237hg38UCSC Ensembl
chr5:162643755..162663243hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3819489
hg1919489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325238
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238729
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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