A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170827



Internal ID22330954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120143877..120143955hg38UCSC Ensembl
chrX:119277783..119277861hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14403253
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)nsv3170827
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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