A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10029n152



Internal ID22825732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730198..9730376hg38UCSC Ensembl
chrX:9698238..9698416hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3178585, nsv3179606
SamplesHG00733, HG00514
Known GenesGPR143
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10029n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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