A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14317486



Internal ID22316696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145693831..145694571hg38UCSC Ensembl
chr4:146614983..146615723hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3546159
Supporting Variants
SamplesNA19240
Known GenesC4orf51
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14317486
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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