A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230668



Internal ID22371996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49157254..49162986hg38UCSC Ensembl
chrX:49013593..49019324hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385733
hg195732
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351177, nssv14351175, nssv14351183, nssv14351180, nssv14351181, nssv14351182, nssv14351178, nssv14351179, nssv14351176
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesMAGIX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230668
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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