A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186343



Internal ID22339142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3876299..3914728hg38UCSC Ensembl
chrX:3794340..3832769hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3838430
hg1938430
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14413342
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186343
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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