A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10027n152



Internal ID22825730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9388955..9389744hg38UCSC Ensembl
chrX:9356995..9357784hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3189036, nsv3178788
SamplesHG00733, 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)dgv10027n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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