A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186195



Internal ID22339065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78202705..78203938hg38UCSC Ensembl
chrX:77458202..77459435hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10163n152
Supporting Variantsnssv14404013
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186195
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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