A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190543



Internal ID22341394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123253813..123256675hg38UCSC Ensembl
chr10:125013329..125016191hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382863
hg192863
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1083n152
Supporting Variantsnssv14382331, nssv14379485
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)nsv3190543
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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