A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194191



Internal ID22344539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123253719..123256774hg38UCSC Ensembl
chr10:125013235..125016290hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383056
hg193056
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1083n152
Supporting Variantsnssv14413207, nssv14413208
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)nsv3194191
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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