A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181456



Internal ID22336581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110705431..110705574hg38UCSC Ensembl
chrX:109948659..109948802hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10235n152
Supporting Variantsnssv14461836, nssv14404400
SamplesNA19240, HG00733
Known GenesCHRDL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181456
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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