A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187608



Internal ID22339818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154634753..154646444hg38UCSC Ensembl
chrX:153863019..153874718hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3811692
hg1911700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439340
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)nsv3187608
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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