A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189036



Internal ID22340568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9388955..9389742hg38UCSC Ensembl
chrX:9356995..9357782hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10027n152
Supporting Variantsnssv14429061
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)nsv3189036
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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