A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178884



Internal ID22335245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17752363..17752472hg38UCSC Ensembl
chrX:17770483..17770592hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14404258
SamplesNA19240
Known GenesSCML1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178884
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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