A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188048



Internal ID22340049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26246662..26246725hg38UCSC Ensembl
chrX:26264779..26264842hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459956
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188048
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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