A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10014n152



Internal ID22825717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5047705..5057178hg38UCSC Ensembl
chrX:4965746..4975219hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg389474
hg199474
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3178153, nsv3178730, nsv3177172
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10014n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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