A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14312154



Internal ID22233222
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3245533
Supporting Variants
SamplesHG00733
Known GenesMIR572
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14312154
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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