A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3551761



Internal ID22420667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61785368..62149739hg38UCSC Ensembl
chr9:44958294..45250204hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38364372
hg19291911
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462057, nssv14458234, nssv14459552, nssv14452901, nssv14458312, nssv14466614, nssv14464384, nssv14455335, nssv14465473
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesFAM27C
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3551761
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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