A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207213



Internal ID22355641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119488574..119489058hg38UCSC Ensembl
chrX:118622537..118623021hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352669, nssv14352670, nssv14352668
SamplesHG00732, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207213
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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