A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218549



Internal ID22363855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93027451..93028700hg38UCSC Ensembl
chr9:95789733..95790982hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9664n152
Supporting Variantsnssv14348928, nssv14348932, nssv14348925, nssv14348926, nssv14348924, nssv14348927, nssv14348929, nssv14348931, nssv14348930
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesFGD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218549
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer