A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10326n152



Internal ID22826029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141906090..141906301hg38UCSC Ensembl
chrX:140993876..140994087hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3199715, nsv3205215
SamplesHG00731, HG00732, HG00733
Known GenesMAGEC1
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10326n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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