A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3546159



Internal ID22415157
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6874n152
Supporting Variantsnssv14317478, nssv14317483, nssv14317480, nssv14317482, nssv14317481, nssv14317484, nssv14317485, nssv14317479, nssv14317486
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesC4orf51
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3546159
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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