A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10096n152



Internal ID22825799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42473374..42475078hg38UCSC Ensembl
chrX:42332626..42334330hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3279924, nsv3197675
SamplesHG00512, NA19238, NA19239, HG00731, NA19240
Known Genes
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)dgv10096n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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