A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3245533



Internal ID22376175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11235281..11384708hg38UCSC Ensembl
chr4:11236905..11386332hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38149428
hg19149428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312153, nssv14312154
SamplesHG00731, HG00733
Known GenesMIR572
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3245533
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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