A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10031n152



Internal ID22825734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9791968..9792076hg38UCSC Ensembl
chrX:9760008..9760116hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3280122, nsv3279833, nsv3282463
SamplesNA19240, HG00733, HG00514
Known GenesSHROOM2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10031n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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