A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6874n152



Internal ID22822577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145693712..145694599hg38UCSC Ensembl
chr4:146614864..146615751hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3545366, nsv3546159
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesC4orf51
MethodSequencing
AnalysisMultiple analysis algorthms
Single strand sequencing, and assortment analysis
PlatformIllumina HiSeq
Strand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6874n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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