A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173124



Internal ID22332166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103525123..103525183hg38UCSC Ensembl
chrX:102780051..102780111hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412617
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)nsv3173124
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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