A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10109n152



Internal ID22825812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46498861..46499236hg38UCSC Ensembl
chrX:46358296..46358671hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3193546, nsv3200243
SamplesNA19238, HG00731, NA19240
Known GenesZNF674
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)dgv10109n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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